CPP Investment Board

The Canada Pension Plan Investment Board, operating as CPP Investments, is a Canadian Crown corporation established by way of the 1997 Canada Pension Plan Investment Board Act to oversee and invest the funds contributed to and held by the Canada Pension Plan.

The CPP Investment Board began its investing program in 1999, establishing the CPP Reserve Fund to hold investment earnings and CPP contributions not needed to pay current pensions.

The CPP Investment Board’s mandate is laid out in its founding legislation, the Canada Pension Plan Investment Board Act.

The CPP reserve fund seeks to achieve at least the projected return needed to help sustain the CPP , a rate set at 4.0% by 2017 in the CPP actuary’s report, starting from 3.2% in 2011.

As indicated in its Financial Highlights for the fiscal year ended March 31, 2013, the CPP reserve fund averaged 4.2% return in the past 5 years, and a 7.4% return in the past 10 years, above the sum of projected Canadian inflation rates and the 4.0% target identified by the CPP Actuary report, or 6.3% in nominal basis, that is required for CPP contribution sustainability.

The CPP Investment Board hires private equity firms to help it invest in private companies, fund managers to help it invest in public equities, bond managers to assist in investing in bonds, and so forth.

The total growth of the CPP Reserve Fund is derived from the CPP contributions of working Canadians, and the return on investment of the contributions.

Canada Pension Plan Investments

Canada Pension Plan Investments is a global investment management organisation established to help ensure the Canada Pension Plan is strong and sustainable for the long term.

The CPP Investment Board was established by an Act of Parliament in December 1997.

CPP invest around the world in public and private assets.

Investments are diversified by asset class and geography so that the Fund is more resilient, and to safeguard the best interests of current and future CPP beneficiaries.

Investments are diversified by asset class and geography so that the Fund is more resilient.

CPP Investment Board

Canada Pension Plan Investment Board is a professional investment management organization with a critical purpose – to help provide a foundation on which Canadians build financial security in retirement.

We invest the assets of the Canada Pension Plan not currently needed to pay pension, disability and survivor benefits.

CPP Investments Partners Up With Inpher To Develop Unique Datasets

“Working with Inpher to leverage their technology to access non-public data sources aligns with our objective to enhance our informational edge and generate value for the CPP Fund over the long run,” said Daniel Wroblewski, managing director and head of CPP Investments’ Alpha Generation Lab, which looks for creative new ways to increase investment returns.

Through this data privacy approach – and the development of a scalable data collaboration network – CPP Investments and Inpher seek to bring together a group of asset managers and data contributors to generate new insights.

Through this collaboration, CPP Investments will work closely with various organizations to incorporate new data sources into forecasting and investment decision-making, while keeping that data private and secure.

“Working with Inpher to leverage their technology to access non-public data sources aligns with our objective to enhance our informational edge and generate value for the CPP Fund over the long run,” said Daniel Wroblewski, Managing Director, Head of CPP Investments’ Alpha Generation Lab, which seeks transformational ways to deliver strong financial performance.

Inpher and CPP Investments aim to establish a trusted network of partners, including traditional data suppliers, corporates, and peer investors, to improve our collective ability to leverage data assets.

The Lab’s mandate is to develop significant advantages for CPP Investments in the search for outsized investment performance by accelerating innovative investment capabilities focused on technology and data.

Inpher and CPP Investments aim to establish a trusted network of partners, including traditional data suppliers, corporates, and peer investors, to improve their collective ability to leverage data assets.

Irritable Bowel Syndrome

Only a small number of people with IBS have severe signs and symptoms.

IBS doesn’t cause changes in bowel tissue or increase your risk of colorectal cancer.

See your doctor if you have a persistent change in bowel habits or other signs or symptoms of IBS. They may indicate a more serious condition, such as colon cancer.

People exposed to stressful events, especially in childhood, tend to have more symptoms of IBS. Changes in gut microbes.

A true food allergy rarely causes IBS. But many people have worse IBS symptoms when they eat or drink certain foods or beverages, including wheat, dairy products, citrus fruits, beans, cabbage, milk and carbonated drinks.

Most people with IBS experience worse or more-frequent signs and symptoms during periods of increased stress.

Estrogen therapy before or after menopause also is a risk factor for IBS. Have a family history of IBS. Genes may play a role, as may shared factors in a family’s environment or a combination of genes and environment.

Irritable Bowel Syndrome

Irritable bowel syndrome is a group of symptoms that occur together, including repeated pain in your abdomen and changes in your bowel movements, which may be diarrhea, constipation, or both.

The most common symptoms of irritable bowel syndrome are pain in your abdomen, often related to your bowel movements, and changes in your bowel movements.

Doctors aren’t sure what causes IBS. To diagnose irritable bowel syndrome, doctors review your symptoms and your medical and family history and perform a physical exam.

Doctors may treat irritable bowel syndrome by recommending changes in what you eat and other lifestyle changes, medicines, probiotics, and mental health therapies.

Your doctor may recommend changes in your diet to help treat symptoms of irritable bowel syndrome.

Changes may include eating more fiber, avoiding gluten, or following a special diet called the low FODMAP diet.

Different changes may help different people with IBS. The National Institute of Diabetes and Digestive and Kidney Diseases and other components of the National Institutes of Health conduct and support research into many diseases and conditions.

Irritable Bowel Syndrome

Disorders such as anxiety, major depression, and chronic fatigue syndrome are common among people with IBS. IBS does not lead to malabsorption.

The primary symptoms of IBS are abdominal pain or discomfort in association with frequent diarrhea or constipation and a change in bowel habits.

The stress response in the body involves the hypothalamic-pituitary-adrenal axis and the sympathetic nervous system, both of which have been shown to operate abnormally in people with IBS. Psychiatric illness or anxiety precedes IBS symptoms in two-thirds of people with IBS, and psychological traits predispose previously healthy people to developing IBS after gastroenteritis.

IBS occurs in 51% of people with chronic fatigue syndrome and 49% of people with fibromyalgia, and psychiatric disorders occur in 94% of people with IBS. Channelopathy and muscular dystrophy: IBS and functional GI diseases are comorbidities of genetic channelopathies that cause cardiac conduction defects and neuromuscular dysfunction, and result also in alterations in GI motility, secretion, and sensation.

Inflammatory bowel disease: IBS may be marginally associated with inflammatory bowel disease.

Some yogurt is made using probiotics that may help ease symptoms of IBS. A probiotic yeast called Saccharomyces boulardii has some evidence of effectiveness in the treatment of irritable bowel syndrome.

There is increasing evidence for the effectiveness of mesalazine in the treatment of IBS. Mesalazine is a drug with anti-inflammatory properties that has been reported to significantly reduce immune mediated inflammation in the gut of IBS affected individuals with mesalazine therapy resulting in improved IBS symptoms as well as feelings of general wellness in IBS affected people.

Irritable Bowel Syndrome: IBS, Symptoms, Causes, Treatment

Irritable bowel syndrome, or IBS, is a group of symptoms that affect your digestive system.

Certain medicines only work for certain types of IBS. Often, people with IBS have normal bowel movements some days and abnormal ones on other days.

IBS with mixed bowel habits: You have both hard and lumpy bowel movements and loose and watery movements on the same day.

Women with IBS may find that symptoms flare up during their periods.

No specific therapy works for everyone, but most people with IBS can find a treatment that works for them.

Your healthcare provider will personalize your IBS treatment plan for your needs.

There’s no cure for IBS. The goal of treatment is to control and manage symptoms.

Irritable Bowel Syndrome Symptoms, Causes, Treatments, Medications

If it’s IBS, you’ll likely have these symptoms weekly for 3 months, or less often for at least 6 months.

Women with IBS may have more symptoms during their period.

While several things are known to trigger IBS symptoms, experts don’t know what causes the condition.

It’s not clear what comes first – the stress or the IBS. But there’s evidence that stress management and behavioral therapy can help relieve symptoms in some people with the condition.

There’s no proof any of these foods cause IBS, but they may trigger symptoms.

Food intolerance: Certain foods can make your IBS symptoms worse.

Malnourishment: Cutting back on some types of foods can ease your IBS symptoms.

IBS: Symptoms, Causes, Diagnosis, Triggers, And Treatment

Learn more about the symptoms of IBS. Women may tend to have symptoms around the time of menstruation, or they may have more symptoms during this time.

Learn more about the process of diagnosing IBS. Certain home remedies or lifestyle changes may help to relieve your IBS symptoms without the use of medication.

Learn more about how certain foods interact with IBS symptoms.

Some drugs are used to treat all symptoms of IBS, while other drugs are focused on specific symptoms.

For many people, the key to managing IBS symptoms is to avoid triggers.

Certain foods as well as stress and anxiety can be triggers for IBS symptoms for many people.

IBS with constipation is a type of IBS that typically affects adolescents and young adults.

Irritable Bowel Syndrome

IBS or Irritable Bowel Syndrome is a disorder that is characterized by abdominal discomfort or pain.

Dr. Osler used the phrase mucous colitis to describe IBS. Other terms that have been used are spastic colon, irritable colon, and nervous colon.

In general, people with IBS feel bowel distention with smaller amounts of gas or fecal contents.

Use of the Rome III criteria tends to result in lower reported rates of IBS. As a generality, communities and cultures where there is a level of higher perceived stress, lower quality of life and fewer barriers to accessing health care will report higher numbers of IBS diagnoses, but IBS exists in every country of the world with the higher rates appearing in Nigeria, Iceland, England, Ireland, Greece, Russia, Columbia, Peru, Brazil, the US, New Zealand, Pakistan, South Korea and Malaysia.

The risk of IBS increases if someone in the family has been diagnosed with IBS. The coexistence of depression, anxiety, PTSD or panic disorder has already been mentioned, but IBS is also associated with other disorders-about half of people with IBS also have fibromyalgia, chronic fatigue syndrome, chronic back pain, chronic pelvic pain, chronic headache, and temporomandibular joint dysfunction.

There are a number of chemical messengers which appear to have altered levels in IBS. Reproductive hormones appear to affect IBS as well-changing levels of reproductive hormones during the menstrual cycle can affect the symptoms of IBS. Family history or genetics.

It is not clear how or why these may be associated with IBS. The Forms or Types of Irritable Bowel Syndrome.

European Commission

The European Commission is the executive branch of the European Union.

The European Commission derives from one of the five key institutions created in the supranational European Community system, following the proposal of Robert Schuman, French Foreign Minister, on 9 May 1950.

The Barroso Commission was also the first full Commission since the enlargement in 2004 to 25 members; hence, the number of Commissioners at the end of the Prodi Commission had reached 30.

The treaty further provides that the most recent European elections should be “Taken into account” when appointing the President of the European Commission, and although they are still proposed by the European Council; the European Parliament “Elects” candidates to the office, rather than “Approves” them as under the Treaty of Nice.

Through Article 17 of the Treaty on European Union the commission has several responsibilities: to develop medium-term strategies; to draft legislation and arbitrate in the legislative process; to represent the EU in trade negotiations; to make rules and regulations, for example in competition policy; to draw up the budget of the European Union; and to scrutinise the implementation of the treaties and legislation.

The President of the Commission is first proposed by the European Council, following a Qualified Majority Vote, taking into account the latest Parliamentary elections; that candidate then faces a formal election in the European Parliament.

In September 2020, the European Commission put forward an Anti-Racism Action Plan to tackle the structural racism in the European Union, including measures to address the lack of racial diversity among the European decision makers in Brussels, as denounced by #BrusselsSoWhite.

Fact Sheets On The European Union

It is the principal executive body of the European Union and is formed by a College of members composed of one Commissioner per Member State.

Article 17 of the Treaty on European Union, Articles 234, 244 to 250, 290 and 291 of the Treaty on the Functioning of the European Union, and the Treaty Establishing a Single Council and a Single Commission of the European Communities.

The Treaty of Lisbon stipulates that the results of the European elections have to be taken into account when the European Council, after appropriate consultations and TEU as an annex to the Treaty) and acting by a qualified majority, proposes the candidate for President of the Commission to Parliament.

The President and the other members of the Commission, including the High Representative of the Union for Foreign Affairs and Security Policy, are subject to a vote of consent, as a body, by Parliament and are then appointed by the European Council, acting by a qualified majority.

The Commission is collectively accountable to Parliament under Article 234 TFEU. If Parliament adopts a motion of censure against the Commission, all of its members are required to resign, including the High Representative of the Union for Foreign Affairs and Security Policy as far as his or her duties in the Commission are concerned.

In this area, many competences have been transferred from the Commission to the High Representative of the Union for Foreign Affairs and Security Policy and the European External Action Service.

The Commission is also consulted, in particular, about changes in the statutes of other institutions and bodies, such as the Statute for Members of the European Parliament, of the European Ombudsman and of the Court of Justice.

European Commission

European Commission, an institution of the European Union and its constituent entities that makes up the organization’s executive arm.

The EC is composed of members called commissioners, who are citizens of and are nominated by the respective governments of each member state.

The EC is charged with representing the EU or community interest, not the interests of the member states, and the commissioners are called to act independently in that interest.

The EC is made up of one member from each of the EU’s 27 member states.

One of the treaty’s key provisions was to reduce the number of commissioners to two-thirds of that number by 2014 so that thereafter member states would provide the EC with commissioners on a rotating basis.

The procedure is that the governments of the member states jointly select a commission president, who is then approved by Parliament.

The commission president-designate, in discussion with the member state governments, chooses the other members of the EC. The new Parliament then interviews each member and gives its opinion on the new EC as a body.

European Commission

The European Commission is the EU’s politically independent executive arm.

It is alone responsible for drawing up proposals for new European legislation, and it implements the decisions of the European Parliament and the Council of the EU.What does the Commission do?Proposes new laws.

Political leadership is provided by a team of 27 Commissioners – led by the Commission President, who decides who is responsible for which policy area.

The College of Commissioners is composed of the President of the Commission, eight Vice-Presidents, including three Executive Vice-Presidents, the High Representative of the Union for Foreign Affairs and Security Policy, and 18 Commissioners, each responsible for a portfolio.

The day-to-day running of Commission business is performed by its staff, organised into departments known as Directorates-General, each responsible for a specific policy area.

The current Commission’s term of office runs until 31 October 2024.How does the Commission work?Strategic planning.

The President defines the policy direction for the Commission, which enables the Commissioners together to decide strategic objectives, and produce the annual work programme.

Rockridge Resources Ltd.

Mr. Gallucci is a senior capital markets executive and corporate director with over 20 years of experience in investment banking and equity research.

His career focused on mining, base metals, precious metals and bulk commodities on a global scale.

He is currently the Managing Director and Head of Investment Banking at Laurentian Bank Securities Inc. where he oversees the investment banking practice in entirety.

His career has spanned across various firms including BMO Capital Markets, GMP Securities, Dundee Securities, and he was a founding principal of Eight Capital where he led their Mining Investment Banking Team.

Prior to investment banking, Mr. Gallucci spent over a decade in equity research with a focus on global mining at both GMP and Dundee Securities.

At Dundee Securities, he was a Managing Director and Head of the Metals and Mining Research Team, where he oversaw the entire mining franchise.

He holds a Bachelor of Commerce degree from Concordia University and an MBA in Investment Management from the Goodman Institute of Investment Management.

Rockridge Resources Ltd. Stock Quote

Rockridge Resources Ltd. is a junior exploration stage company, which engages in the acquisition and development of mineral property interests.

The company was founded by Jordan Trimble on November 10, 2015 and is headquartered in Vancouver, Canada.

Rockridge Resources Completes Oversubscribed Non-Brokered Financing

Over the last 100 years, the Flin-Flon mining camp in Manitoba and Saskatchewan has produced over 180 million tons of sulphide ore from over 35 VMS deposits worth in excess of $30 billion dollars.

Rockridge also owns 100% of the Raney Gold Project, which is attractively positioned near the world-class Timmins and Kirkland Lake lode gold mining camps in Ontario.

The company is currently advancing its large, 55,471 hectare, flagship Knife Lake project in the Flin Flon-Snow Lake mining district on the Saskatchewan side of the border.

6 billion has been invested into mine development in the surrounding Flin Flon district and over 50% of deposits in the Flin Flon district have been advanced to production, which have led to nearly 100 consecutive years of mining.

Hudbay operates the several mines nearby, and recently discovered a new high-grade zinc zone between the two mines Chisel North and Lalor.

Throughout his career, Trimble has founded and helped manage several public and private companies and has been instrumental in raising substantial capital for mining companies with his extensive network of institutional and retail investors.

At Dundee Securities, he was a managing director and head of the Metals and Mining Research Team, where he oversaw the entire mining franchise.

VBI Vaccines Stock Rating Upgraded By Zacks Investment Research

VBI Vaccines was upgraded by Zacks Investment Research from a “Sell” rating to a “Hold” rating in a research report issued to clients and investors on Tuesday, Zacks.com reports.

According to Zacks, “VBI Vaccines Inc. is a biopharmaceutical company developing novel technologies to expand vaccine protection. The company’s eVLP vaccine platform allows for the design of enveloped virus-like particle vaccines which closely mimic the target virus. Its lead eVLP asset is a prophylactic cytomegalovirus vaccine. Its second platform is a thermostable technology that enables the development of vaccines and biologics. VBI Vaccines Inc., formerly known as SciVac Therapeutics, Inc., is headquartered in Cambridge, MA.”.

Raymond James lowered their price objective on VBI Vaccines from $9.00 to $6.00 and set a “Strong-buy” rating on the stock in a research note on Tuesday, March 8th. Jefferies Financial Group assumed coverage on shares of VBI Vaccines in a research report on Thursday, December 30th. They set a “Buy” rating and a $6.00 price target on the stock.

Shares of VBI Vaccines stock traded down $0.06 during trading hours on Tuesday, reaching $1.76.

As a group, research analysts predict that VBI Vaccines will post -0.31 EPS for the current year.

VBI Vaccines Inc, a biopharmaceutical company, develops and sells vaccines for the treatment of infectious diseases and immuno-oncology.

Get a free copy of the Zacks research report on VBI Vaccines.

VBI Vaccines Stock Rating Upgraded By Zacks Investment Research

VBI Vaccines was upgraded by Zacks Investment Research from a “Sell” rating to a “Hold” rating in a research report issued to clients and investors on Tuesday, Zacks.com reports.

According to Zacks, “VBI Vaccines Inc. is a biopharmaceutical company developing novel technologies to expand vaccine protection. The company’s eVLP vaccine platform allows for the design of enveloped virus-like particle vaccines which closely mimic the target virus. Its lead eVLP asset is a prophylactic cytomegalovirus vaccine. Its second platform is a thermostable technology that enables the development of vaccines and biologics. VBI Vaccines Inc., formerly known as SciVac Therapeutics, Inc., is headquartered in Cambridge, MA.”.

Raymond James lowered their price objective on VBI Vaccines from $9.00 to $6.00 and set a “Strong-buy” rating on the stock in a research note on Tuesday, March 8th. Jefferies Financial Group assumed coverage on shares of VBI Vaccines in a research report on Thursday, December 30th. They set a “Buy” rating and a $6.00 price target on the stock.

Shares of VBI Vaccines stock traded down $0.06 during trading hours on Tuesday, reaching $1.76.

As a group, research analysts predict that VBI Vaccines will post -0.31 EPS for the current year.

VBI Vaccines Inc, a biopharmaceutical company, develops and sells vaccines for the treatment of infectious diseases and immuno-oncology.

Get a free copy of the Zacks research report on VBI Vaccines.

VBI Vaccines Announces New Data And Progress Of VBI-2900, VBI’S EVLP Coronavirus Program

VBI Vaccines Inc., a biopharmaceutical company driven by immunology in the pursuit of powerful prevention and treatment of disease, today announced updated clinical and preclinical data from its coronavirus program, VBI-2900.

Dr. Melanie Saville, Executive Director of Vaccine R&D, CEPI, said: “Over the last two years, we have seen the persistent evolution of SARS-CoV-2. To stay one-step ahead of SARS-CoV-2 variants and other deadly coronaviruses, the world must invest in multivalent, broadly protective coronavirus vaccine technologies-like the eVLP technology being advanced by VBI. These data represent an important first step in the evaluation of this technology and toward developing an effective vaccine platform against variants of concern and other coronavirus threats.”

The new clinical and preclinical data for all three candidates have continued to support the robust potential of the eVLP platform, with candidates that have been able to elicit broad immune responses against coronaviruses.

VBI-2902 and VBI-2905 were evaluated at a low dose of 5µg and both are adjuvanted with aluminum phosphate, a well-known adjuvant with decades of safety data from multiple FDA-approved vaccines.

About VBI’s Coronavirus Vaccine Program: VBI-2900 VBI-2900 consists of three enveloped virus-like particle vaccine candidates: VBI-2901, a trivalent pan-coronavirus vaccine expressing the SARS-CoV-2, SARS-CoV, and MERS-CoV spike proteins, VBI-2902, a monovalent COVID-19 vaccine expressing a modified prefusion form of the SARS-CoV-2 spike protein, and VBI-2905, a monovalent COVID-19 vaccine expressing a modified prefusion form of the spike protein from the Beta variant.

About VBI Vaccines Inc. VBI Vaccines Inc. is a biopharmaceutical company driven by immunology in the pursuit of powerful prevention and treatment of disease.

Through its innovative approach to virus-like particles, including a proprietary enveloped VLP platform technology, VBI develops vaccine candidates that mimic the natural presentation of viruses, designed to elicit the innate power of the human immune system.

VBI Vaccines Announces PreHevbrio(TM) Is Now Available In The United States For The Prevention Of Hepatitis B In Adults

PreHevbrio™ is the only approved 3-antigen hepatitis B vaccine for adults in the U.S. – FDA approval of PreHevbrio received in November 2021 – PreHevbrio added to ACIP list of recommended adult HBV vaccines in February 2022 – Wholesale Acquisition Cost set at $64.75/dose.

VBI Vaccines Inc., a biopharmaceutical company driven by immunology in the pursuit of powerful prevention and treatment of disease, today announced that PreHevbrio™ is now available in the United States for the prevention of infection caused by all known subtypes of hepatitis B virus in adults age 18 years and older.

“We are proud to announce the U.S. availability of PreHevbrio, a significant milestone in our effort to be part of the fight against hepatitis B,” said Jeff Baxter, VBI’s President and CEO.”This launch coincides with the swell of momentum following the ACIP’s November 2021 unanimous vote to move to a universal HBV vaccination recommendation for all adults age 19-59, and its February 2022 decision to include PreHevbrio in its list of recommended adult HBV vaccines.

PreHevbrio is indicated for prevention of infection caused by all known subtypes of hepatitis B virus.

Do not administer PreHevbrio to individuals with a history of severe allergic reaction after a previous dose of any hepatitis B vaccine or to any component of PreHevbrio.

PreHevbrio may not prevent hepatitis B infection, which has a long incubation period, in individuals who have an unrecognized hepatitis B infection at the time of vaccine administration.

VBI’s vaccine candidate is the only 3-antigen hepatitis B vaccine, comprised of the S, pre-S1, and pre-S2 surface antigens of the hepatitis B virus, and is approved for use in the United States under the name PreHevbrio™ , and in Israel under the name Sci-B-Vac®.

VBI Vaccines To Start Clinical Study Of Pan-Coronavirus Vaccine Candidate This Year

VBI Vaccines Inc announced updated clinical and preclinical data from its VBI-2900 coronavirus program, consisting of three candidates.

VBI-2902 and VBI-2905, evaluated at a low dose of 5µg, were well-tolerated in clinical studies, with no safety signals observed.

In the Phase 1b study, a single-dose booster of VBI-2905 increased neutralizing antibodies directed against the Beta variant 3.8-fold in participants who had previously received two doses of an mRNA vaccine.

Approximately 2-fold increases were also seen in antibody levels against the ancestral and delta variant.

Against a panel of coronavirus variants in mice, reactivity was seen with VBI-2902 against all variants, including the ancestral strain, Delta, Beta, Omicron, Lambda, and RaTG13.

In this same panel, VBI-2901 elicited an even stronger response against all variants tested.

VBI-2901 elicited a more significant difference in antibody levels from VBI-2902, ranging from 2.5-fold higher against the ancestral strain to 9.0-fold higher against the bat coronavirus.

VBI Vaccines Announces New Data And Progress Of VBI-2900, VBI’S EVLP Coronavirus Program

CAMBRIDGE, Mass.-(BUSINESS WIRE)- VBI Vaccines, a biopharmaceutical company driven by immunology in the pursuit of powerful prevention and treatment of disease, today announced updated clinical and preclinical data from its coronavirus program, VBI-2900.

Dr. Melanie Saville, Executive Director of Vaccine R&D, CEPI, said: “Over the last two years, we have seen the persistent evolution of SARS-CoV-2. To stay one-step ahead of SARS-CoV-2 variants and other deadly coronaviruses, the world must invest in multivalent, broadly protective coronavirus vaccine technologies-like the eVLP technology being advanced by VBI. These data represent an important first step in the evaluation of this technology and toward developing an effective vaccine platform against variants of concern and other coronavirus threats.”

The new clinical and preclinical data for all three candidates have continued to support the robust potential of the eVLP platform, with candidates that have been able to elicit broad immune responses against coronaviruses.

VBI-2902 and VBI-2905 were evaluated at a low dose of 5µg and both are adjuvanted with aluminum phosphate, a well-known adjuvant with decades of safety data from multiple FDA-approved vaccines.

About VBI’s Coronavirus Vaccine Program: VBI-2900 VBI-2900 consists of three enveloped virus-like particle vaccine candidates: VBI-2901, a trivalent pan-coronavirus vaccine expressing the SARS-CoV-2, SARS-CoV, and MERS-CoV spike proteins, VBI-2902, a monovalent COVID-19 vaccine expressing a modified prefusion form of the SARS-CoV-2 spike protein, and VBI-2905, a monovalent COVID-19 vaccine expressing a modified prefusion form of the spike protein from the Beta variant.

About VBI Vaccines Inc. VBI Vaccines Inc. is a biopharmaceutical company driven by immunology in the pursuit of powerful prevention and treatment of disease.

Through its innovative approach to virus-like particles, including a proprietary enveloped VLP platform technology, VBI develops vaccine candidates that mimic the natural presentation of viruses, designed to elicit the innate power of the human immune system.

VBI Vaccines Stock Price, News & Info

The company reported good news from a study of its hepatitis B vaccine.

“Buy low, sell high” is easy when stocks are cheap.

Here’s why investors should stay away from some of the riskiest coronavirus stocks on the market.

Investors who are looking for promising coronavirus vaccine stocks should keep an eye out for this emerging biotech.

Investors are fired up about an analyst’s enthusiastic upgrade of the biotech stock.

Momentum continued from an upgrade and investors’ attraction to stocks with COVID-19 programs.

Get stock recommendations, portfolio guidance, and more from The Motley Fool’s premium services.

VBI Vaccines

Variation Biotechnologies Inc., also known as VBI Vaccines Inc., is a biopharmaceutical company, headquartered in Cambridge, Massachusetts, with research facilities in Ottawa, Ontario, Canada, and a research and manufacturing site in Rehovot, Israel.

In August VBI received CA$56 million from the Government of Canada to prepare its vaccine for clinical trials by the end of 2020.

The company’s CEO, Jeff Baxter, said that VBI-2902 is cheaper to produce than other vaccines.

According to the company, they have two vaccine candidates-“Enveloped virus-like particle”.

VBI-2901 is a “Trivalent pan-coronavirus vaccine expressing the SARS-CoV-2, SARS-CoV, and MERS-CoV spike proteins”.

VBI-2902 is a “Monovalent COVID-19-specific vaccine expressing the SARS-CoV-2 spike protein”.

VBI received CA$56 million from the federal government towards the COVID-19 vaccine development.

Harvey Water Softeners

Now the largest domestic water softener manufacturer in Europe, Harvey Water Softeners looks forward to further international expansion, and brand-new innovations in sustainable drinking water technology.

Since 1978, Harvey Water Softeners has pioneered the most cutting-edge water softening technology from its manufacturing base in Woking, Surrey.

“Having softer water in your home has a plethora of benefits; softened water is kinder to skin, easier to lather, less damaging to appliances and more cost-effective. Harvey’s selection of domestic water softeners are specifically engineered to enhance all of these benefits, as Gavin Bridger, Head of Operations, summarizes:”Harvey Water Softeners is the UK’s no.1 water softener manufacturer for small commercial and residential applications.

“With a twin cylinder design, which is at the forefront of innovation, the Harvey Water Softener features technology that provides the home with softened water 24/7, and works at optimum efficiency.”

Harvey water softening systems can be tailored to the water needs of each individual customer.

“Harvey Water Softeners prides itself on efficiency, hygiene and quality of service. As Gavin points out:”It is important to us that we provide the most efficient and reliable water softener available today.

“Having emerged successfully from the conditions of a pandemic, Harvey Water Softeners continues to flourish under its new parent company, the Culligan Group. Culligan International is a company that manufactures water treatment products on an international scale, as Gavin explains:”The company produces water purification equipment such as water softener systems, filters, bottle-less coolers, and municipal water conditioners.

Do NOT Buy Until You Read This Harvey’S Water Softener Review

The Harvey’s water softener brand is one of the longest standing and popular brands of water softeners in the UK. When it comes to water, of course, you always want the best quality.

The only way to deal with hard water is with a water softener.

The most effective way to deal with hard water is to use a water softener.

There are tons and tons of different water softeners available on the market today, but which is the best? The following sections will review the water softener offerings from a brand called Harvey.

The Harvey’s Crown softener is a the high end of water softener prices coming in at around £850-£950.

The M2 water softener uses an easy-to-handle 4 kg block salt that simply slides into the front of the softener machine device.

The Harvey water softener surpasses many larger softeners despite only being 49 cm in height.

Harvey Water Softeners

I needed to replace an old water softener and contacted Cotswold Water Softeners on the basis of their excellent reviews – I will add another one! They are a very professional and friendly company, with great communications and punctuality.

The survey was very good, with lots of useful information from Tim.

The installation by Simon was first class, very neat indeed and we’re delighted with the finished product.

HARVEY WATER SOFTENERS LIMITED Company Key Information

According to the latest account statement, there are currently 236 of employees working for HARVEY WATER SOFTENERS LIMITED. How much revenue does HARVEY WATER SOFTENERS LIMITED make?

Based on the latest financial accounts submitted on 2019-12-31, the company made £41M for 2019, which went up by 29.67%. What is HARVEY WATER SOFTENERS LIMITED EBITDA?

For 2019, HARVEY WATER SOFTENERS LIMITED has reported an EBITDA of £4M, which went up by 476.41% compared to previous year.

What is the Business Credit Score of HARVEY WATER SOFTENERS LIMITED and how reliable is the company?

Does HARVEY WATER SOFTENERS LIMITED pay their invoices on time?

By requesting a Business Credit Report for HARVEY WATER SOFTENERS LIMITED, you will be able to gain more insights about the HARVEY WATER SOFTENERS LIMITED payment trends.

Information about the ultimate beneficial ownership HARVEY WATER SOFTENERS LIMITED of HARVEY WATER SOFTENERS LIMITED is available when you order a business credit report.

Harvey Water Softeners

It’s an excellent service, Adam was so good and polite, my water softener running very smoothly so I can’t ask for more.

The engineer undertakes a thorough service of the water softener, checks level of softness in the taps and checks water flow is within expected range.

Installed water softener at my property 1.5 years ago.

We have recently had a water softener installed by Aquasoft.

We are over the moon with the quality of the product, our water is so much better than before! The service we had from Tristan and Adam was great as well.

Happy with the results and the water tastes different from the filtered water tap.

Very pleased with the company and the service they give in looking after our water softener!

Original Equipment Manufacturer Definition

If a person wants to do their own car repairs, they can often buy OEM parts directly from the manufacturer or a retailer who stocks those parts.

One of the most basic examples of an OEM is the relationship between an auto manufacturer and a maker of auto parts.

Parts such as exhaust systems or brake cylinders are manufactured by a wide variety of OEMs. The OEM parts are then sold to an auto manufacturer, which then assembles them into a car.

There is a second, newer definition of OEM, typically used in the computer industry.

In the traditional sense of the term, Microsoft is the OEM and Dell the VAR. However, the computer’s product guide for consumers is most likely to refer to Dell as the OEM. An OEM is the opposite of the aftermarket.

An OEM refers to something made specifically for the original product, while the aftermarket refers to equipment made by another company that a consumer may use as a replacement.

They may buy the OEM part, which is a duplicate of their original ABC thermostat that was used in the original manufacturing of the vehicle.

Original Equipment Manufacturer

An Original Equipment Manufacturer or OEM is a company that manufactures and sells products or parts of a product that their buyer, another company, sells to its own customers while putting the products under its own Brand Equity.

Such as its processor or memory module, may be the products of an OEM.Original Equipment Manufacturer vs. Value-Added Reseller.

The two share a mutually beneficial relationship, as VARs help OEMs sell their products and OEMs entrust their products to VARs, allowing them to sell them with more features that will enhance the operation of the products.

While an Original Equipment Manufacturer produces original equipment, an aftermarket manufacturer, on the other hand, makes products that are made to look like and work interchangeably with those of the OEM. In simpler terms, the parts are not original products because they’ve been manufactured by companies, locally-based or foreign-based, without approval from the OEMs to produce such products.

The products are not guaranteed to function as well as the OEM product.

Hardware can be easily bought off the internet, whether from a retail product manufacturer or through an OEM. However, OEM hardware is usually shipped incomplete of parts such as cables and adapters that are necessary for the installation and operation of the hardware.

Why not? After all, an OEM product is the same product manufactured by the original manufacturer.

What Is An Original Equipment Manufacturer?

A company which, with its own facilities, performs the primary activities in transforming inorganic or organic substances, including the assembly of parts and components, into the end item being acquired.

For commodities, an OEM is normally a company that builds a commodity product or component and incorporates it into a new product with its own brand name and derives at least 40% of its revenue from products that are manufactured by the OEM;.

For managed services, an OEM is normally a company that derives at least 40% of its revenue from Data Processing, hosting, and related services;.

For telecommunications, and OEM is normally a company that derives at least 40% of its revenue from wired telecommunications carriers.

An OEM may make complete devices or just certain components, either of which can then be configured by the reseller.

OEMS TODAY. Today, component parts and processed items are becoming branded, and as such their names are becoming well-known by consumers.

In the past, these components were processed from raw materials and became part of a finished product without the consumer ever becoming aware of who made the component.

SETTING STANDARDS. Manufacturers must determine the quality and specify standards for components that go into their products.

Some assembled products are not manufactured but put together from a variety of purchased component parts, like Dell computers.

Because components become part of an organization’s own product, quality is extremely important.

Since component parts go into finished products, a replacement market often develops on its own.

Original Equipment Manufacturer

An original equipment manufacturer is generally perceived as a company that produces parts and equipment that may be marketed by another manufacturer.

When referring to auto parts, OEM refers to the manufacturer of the original equipment, that is, the parts assembled and installed during the construction of a new vehicle.

In contrast, aftermarket parts are those made by companies other than the OEM, which might be installed as replacements after the car comes out of the factory.

If Ford used Autolite spark plugs, Exide batteries, Bosch fuel injectors, and Ford’s own engine blocks and heads when building a car, then car restorers and collectors consider those to be the OEM parts.

Any given brand of part can be OEM on some vehicle models and aftermarket on others.

They are primarily for PC manufacturer OEMs and system builders, and as such are typically sold in volume licensing deals to a variety of manufacturers.

System builders also have a different requirement regarding installation media from Direct OEMs. While a clean retail media of Windows can be installed and activated on these devices with OEM keys, actual OEM recovery media that was created by the PC manufacturer typically only works on the PC model line that was designed for it.

Preliminary NA Class 8 net orders in February were 21,000 units, while NA Classes 5-7 net orders rose to 18,300 units.

Complete industry data for February, including final order numbers, will be published by ACT Research in mid-March.

ACT’s State of the Industry: Classes 5-8 Vehicles report provides a monthly.

Transportation Research Center

Because shaping the future of transportation is no accident Innovation Our people are who make TRC a leader in automotive testing and future technology solutions.

People who look, not at where they are, but where they’ve yet to go.

People who are driven, not by what they’ve done, but by what they’ve yet to do.

People who not only seize the present, but imagine tomorrow.

Together, with you, we’re shaping the future of transportation.

TRC’s Instrumentation Calibration Laboratory provides highly accurate and expeditious calibration services for your testing and measurements equipment.

People who not only seize the present, but imaging tomorrow.

American Commercial Barge Line

American Commercial Barge Line is one of the largest and most diversified marine transportation companies in the U.S. Our legacy of providing the nation with the most economical, safest and greenest mode of transportation dates all the way back to 1915, when we began moving coal on the Kentucky River.

At ACBL, OUR MISSION is to deliver safe, innovative marine transportation solutions while empowering Team Members and maximizing stakeholder value.

OUR VISION is to be the Trusted Leader in Marine Transportation.

OUR PRIORITY is always the safety of our Team Members, the marine environment and our customers’ cargoes.

Barium Sulfate

Although barium is a heavy metal, and its water-soluble compounds are often highly toxic, the low solubility of barium sulfate protects the patient from absorbing harmful amounts of the metal.

BaSO4 + 4 C BaS + 4 CO. In contrast to barium sulfate, barium sulfide is soluble in water and readily converted to the oxide, carbonate, and halides.

In the laboratory barium sulfate is generated by combining solutions of barium ions and sulfate salts.

Because barium sulfate is the least toxic salt of barium due to its insolubility, wastes containing barium salts are sometimes treated with sodium sulfate to immobilize the barium.

Barium sulfate is one of the most insoluble salts of sulfate.

Barium sulfate is reduced to barium sulfide by carbon.

Although soluble salts of barium are moderately toxic to humans, barium sulfate is nontoxic due to its insolubility.

Barium Sulfate: MedlinePlus Drug Information

If you are taking barium sulfate by mouth, you may be given the medication after you arrive at the testing center or you may be given the medication to take at home at specific times the night before and/or the day of your test.

If you are taking barium sulfate at home, take it exactly as directed.

Before taking or using barium sulfate,tell your doctor and the staff at the testing center if you are allergic to barium sulfate, other radiopaque contrast media, simethicone, any other medications, any foods, latex, or any of the ingredients in the type of barium sulfate that you will be taking or using.

Your doctor will tell you whether you should take your medications on the day of your test and whether you should wait a certain amount of time between taking your regular medications and taking barium sulfate.

Your doctor may tell you or your child not to take barium sulfate.

If you were given barium sulfate to take at home and you forgot to take a dose, take the missed dose as soon as you remember it.

Tell the staff at the testing center if you did not take the barium sulfate at the scheduled time.

Barium Sulfate Oral/Rectal Uses, Side Effects & Warnings

Dosage forms: oral capsule; oral cream; oral paste; oral powder for reconstitution; oral suspension; oral tablet; oral and rectal powder for reconstitution; oral and rectal suspensionDrug class: Non-iodinated contrast media.

Barium sulfate works by coating the inside of your esophagus, stomach, or intestines which allows them to be seen more clearly on a CT scan or other radiologic examination.

Barium sulfate is used to help diagnose certain disorders of the esophagus, stomach, or intestines.

You should not use barium sulfate if you are allergic to barium sulfate or another contrast agent.

If you receive barium sulfate as a rectal enema, a healthcare professional will give you the medicine at the clinic or hospital where your testing will take place.

You may need to begin taking oral barium sulfate at home, a day before your medical test.

If you are using barium sulfate at home, call your doctor for instructions if you miss a dose.

Properties, Uses, Side Effects And Formula

Pure barium sulfate is found as a white, odorless powder or small crystals with a density of 4.49 g/mL, a melting point of 1580 °C and a boiling point of 1600 °C.Chemical Properties.

Barium sulfate has numerous medical and radio imaging uses due to its water insolubility and radio-opaque properties.

Barium Sulfate Side Effects You should go for emergency medical assistance if you have indications of a hypersensitive response: hives; troublesome breathing; expanding of your face, lips, tongue, or throat.

Barium sulfate is a significant inorganic chemical with several applications, including medical uses.

Structure and Formula of barium sulfate: The chemical formula of barium sulfate is BaSO4 and its molar mass is 233.43 g/mol.

Occurrence: Barium sulfate occurs naturally as the mineral barite, which is widely found and can be considered as the major source of barium and other barium compounds.

If you wish to learn about the formula of the Barium Sulphate then you may like to follow this link.

Structure, Properties, Molecular Weight & Uses

What is Barium Sulfate? BaSO4 is an inorganic compound with the chemical name Barium Sulfate.

Barium Sulfate is composed of a barium cation and the sulfate anion.

BaSO4 is a sulfate salt of barium and is found as mineral barite.

Barium Sulfate Uses It is used in the casting of copper anode plates as a coating material.

Used as a filler or to modify the consistency in oil paints.

It is used in imaging of the GI tract during barium meal.

Used to diagnose certain disorders of the intestines, stomach, or esophagus.

Connection Chemical, LP

Product Description:Barium Sulfate is a solid white crystalline organic compound.

Barium Sulfate is used in a wide arrange of industries from industrial applications to medicinal uses.

Connection Chemical LP is a professional importer of Barium Sulfate.

Connection Chemical has the capability to stock and sell Barium Sulfate from stocking locations nationwide.

Connection Chemical is a supplier and distributor of Barium Sulfate.

As a supplier of Barium Sulfate, Connection Chemical provides supply chain solutions to partners and customers in numerous industries.

We work with competitive prices and reliable manufacturers of Barium Sulfate.

Barium Sulfate Suppliers USA

Texas TX. BARIUM SULFATE Quick inquiry Where to buy Suppliers range BARIUM SULFATE, Reagent grade, typically 0.7 micron average, BaSO4.

New York NY. BARIUM SULFATE Quick inquiry Where to buy Suppliers range BARIUM SULFATE, 99% pure, super fine, typically 0.7 microns, BaSO4.

Nanoparticles Quick inquiry Where to buy Suppliers range Barium.

Powder Quick inquiry Where to buy Suppliers range Barium.

Quick inquiry Where to buy Suppliers range Palladium on barium.

5% Quick inquiry Where to buy Suppliers range Palladium on Barium.

Texas TX. Human Factor XIII Quick inquiry Where to buy Suppliers range Factor XIII is the zymogenic form of the glutaminyl-peptide g-glutamyl transferase factor XIIIa.

Wikipedia

Jennerex Biotherapeutics, Inc. was an American private biopharmaceutical company that developed the oncolytic viruses JX-594 and JX-929 among others.

The immunostimulatory cytokine GM-CSF is produced from the JX-594 genome following infection, inducing immune response against both the virus and the tumor and enabling lasting tumor immunity.

Finally, JX-594 reduces nutrient supply to tumors through blood vessel destruction.

Elimination of TK from the JX-594 genome restricts viral replication to tumor cells, whereas GM-CSF production facilitates tumor immune response against, and β-gal is included for virus tracking purposes.

Upon comparison of intravenous delivery of JX-594 to intratumoral injection in immunocompetent liver cancer model in rabbits over 7 weeks, it was found that the i.t. treatment reduced the average primary tumor volume from 425 cm3 in control animals to 20 cm3 in i.t.-treated animals, and to 35 cm3 in the i.v. treatment group.

Dense infiltration of with CD4+ and CD8+T lymphocytes into the tumor was observed following intratumoral injection of JX-594.

Jennerex has partnered with Transgene, Green Cross, Lee’s Pharmaceuticals, Rex Medical, and SillaJen for JX-594 development and commercialization.

Jennerex Biotherapeutics

Jennerex is a clinical-stage biotherapeutics company focused on the development of first-in-class, targeted oncolytic products for cancer.

Together, we will co-develop JX-594 worldwide, with Transgene responsible for development costs and for clinical development in its licensed territories, pursuant to the JX-594 global development plan.

Green Cross Corp. We currently have a product development and licensing agreement for JX-594 with Green Cross for the Korean market.

Together we are focused on the development and eventual commercialization of JX-594 for liver cancers and other cancer indications in the Korean market.

We are partnered with Lee’s Pharmaceutical Holdings for JX-594 development and commercialization in China.

We exclusively use Rex Medical Quadra-Fuse needles for intratumoral injections of JX-594 in clinical development, and Rex Medical works collaboratively with us to effectively apply this technology to JX-594 clinical development.

SillaJen, Inc. SillaJen is a biotechnology company established to support collaborations with us in the areas of clinical assay development and services, translational research, and GMP manufacturing for the production of oncolytic viruses.

SillaJen Announces Completion Of Jennerex, Inc. Acquisition

PRNewswire/ – SillaJen, Inc., a privately-held biotherapeutics company focused on the development of targeted oncolytic immunotherapy products for cancer, announced today that it had completed the acquisition of San Francisco.

“The strategic acquisition of Jennerex is a natural evolution of the long-standing collaboration between the two companies, solidifying SillaJen’s position as a global leader in the emerging and exciting field of oncolytic immunotherapy.”

& Hachigian, LLP advised Jennerex, Inc. About Pexa-Vec Pexa-Vec is derived from vaccinia, which has been used for decades as a vaccine in healthy individuals, and is engineered to selectively target cancer cells.

Objective tumor responses have been demonstrated in a variety of cancers including liver, colon, kidney, lung cancer and melanoma.

Pexa-Vec is currently being evaluated in a Phase 2 clinical trial in patients with treatment-refractory colorectal cancer as monotherapy and in combination with irinotecan, and in a Phase 2 clinical trial in treatment-refractory kidney cancer patients.

Hepatocellular Carcinoma: A Global Unmet NeedHepatocellular carcinoma is the fifth most common cancer worldwide and the third leading cause of cancer death, with over 600,000 new cases diagnosed annually resulting in more than 90 percent mortality.

The company’s lead product candidate, Pexa-Vec, is in mid-stage clinical development for the treatment of advanced primary liver cancer, colorectal cancer, kidney cancer and ovarian cancer, and its next generation product candidate, JX-929, is under investigation for a variety of other solid tumors.

Jennerex Biotherapeutics Raises $21.6M For Cancer Therapy

Jennerex Biotherapeutics Inc., which develops oncolytic immunotherapies for solid tumors, said it has raised $21.6 million in a private placement.

Jennerex will use the capital to advance its lead product, Pexa-Vec, a potential treatment for liver, colorectal and kidney cancer.

The investors in the round weren’t disclosed in a news release.

Jennerex, Inc. Presents Positive Phase 2 Trial Of JX-594

PRNewswire/ – Jennerex, Inc., a private, clinical-stage biotherapeutics company focused on the development and commercialization of first-in-class targeted oncolytic immunotherapies, presented Phase 2 clinical data of JX-594 delivered first intravenously and subsequently through intra-tumoral route demonstrating safety as well as disease control and tumor responses in patients with hepatocellular carcinoma.

“Our ability to deliver JX-594 intravenously to liver cancer tumors, further confirmed by these encouraging data, is a key attribute that sets it apart from other therapies in the class of oncolytic immunotherapies,” stated David H. Kirn., M.D., founder, chief medical officer and president of R&D of Jennerex.

“In the Phase 2 trial presented at ILCA, JX-594 demonstrated its ability to selectively target and destroy tumors following intravenous infusion. This finding confirms the ability of JX-594 to target both primary and metastatic, or distant, tumors which we believe is important in this HCC patient population and most cancers.”

“We have treated more than 160 patients with JX-594 to date and are actively enrolling a multinational Phase 2b study in second line treatment of liver cancer patients, a Phase 2 all-IV trial in first line HCC patients, and a Phase 2 study in colorectal cancer. The data presented today build on the growing body of promising clinical data showing that JX-594 has a direct anti-tumor effect and can stimulate an immune response killing cancer cells,” stated Laurent Fischer.

Phase 1 and Phase 2 clinical trials in multiple cancer types to date have shown that JX-594, delivered either directly into tumors or intravenously, induces tumor shrinkage and/or necrosis and is well-tolerated.

Transgene, a member of the Institut Merieux Group, is a publicly traded French biopharmaceutical company dedicated to the development of therapeutic vaccines and immunotherapeutic products in oncology and infectious diseases, and has five compounds in clinical development: TG4010 and JX-594 having completed initial phase II trials, TG4001 in phase IIb trial, TG4040 in phase II trial and TG4023 in phase I trial.

The Company’s lead product JX-594 is currently in an international, randomized Phase 2b clinical trial in patients with advanced primary liver cancer who have failed sorafenib therapy.

De Havilland

Unmatched versatility and value The Dash 8-400 is the most productive turboprop on the market.

Known as the “Network builder” due to its short take-off and landing capabilities and efficient regional operations, it comes equipped with more seats, more legroom, more cargo and offers more flights per day.

This aircraft offers the best of both worlds: fly slower to minimize fuel burn or faster to maximize productivity.

It offers the same trip cost as competing 76-seat turboprops but can be configured to fit a maximum of 90 seats.

When compared to a larger jet aircraft, the trip cost is substantially lower at half the cost.

With more seats, more trips per day and longer maintenance intervals, the Dash 8-400 adds over $8 million more value per aircraft.

De Havilland Canada Dash 8

The De Havilland Canada DHC-8, commonly known as the Dash 8, is a series of turboprop-powered regional airliners, introduced by de Havilland Canada in 1984.

In the 1970s, de Havilland Canada had invested heavily in its Dash 7 project, concentrating on STOL and short-field performance, the company’s traditional area of expertise.

On November 8, 2018, Viking Air parent Longview Aviation Capital Corporation acquired the entire Dash 8 program and the de Havilland brand from Bombardier, in a deal that would close by the second half of 2019.

Viking had already acquired the discontinued de Havilland Canada aircraft model type certificates in 2006.

In January 2019, Longview announced that it would establish a new company in Ontario, reviving the de Havilland Aircraft Company of Canada name, to continue production of the Q400 and support the Dash 8 range.

On June 3, 2019, the sale was closed with the newly formed De Havilland Canada taking control of the Dash 8 program, including the previous -100, -200, and -300 series.

In a press release on October 28, 2007, the company’s president said: “Confidence in the Q400 has diminished considerably and our customers are becoming increasingly doubtful about flying in this type of aircraft. Accordingly, with the Board of Directors’ approval, I have decided to immediately remove Dash 8 Q400 aircraft from service.” The preliminary Danish investigation determined the latest Q400 incident was unrelated to the airline’s earlier corrosion problems, in this particular case caused by a misplaced O-ring found blocking the orifice in the restrictor valve.

De Havilland Canada DHC-8 Dash 8

The De Havilland Aircraft Company of Canada DHC-8 or ‘Dash 8’ is a twin turboprop regional transport passenger aircraft which places its design concept on high performance and low operating costs.

The Dash 8-300 flew in May 1987 and then the stretched Dash 8-400 flew in January 1988.

In 1986, the Canadian Government privatised De Havilland Aircraft Company of Canada, selling the aircraft production facilities and product range to Boeing.

Boeing were themselves in direct competition with the fast-emerging European aircraft manufacturing company Airbus and it simply used the De Havilland Canada name to strengthen its relationships with shared product customers.

When Air Canada announced their intention to purchase Airbus aircraft and amidst various accusations, Boeing reacted by placing De Havilland Canada for sale.

Bombardier Aerospace of Montreal eventually acquired De Havilland Canada in 1992, incorporating the aircraft into their portfolio of feeder airliners.

Eventually, all De Havilland Canada Type Certificates were purchased by Viking Air who successfully put the aircraft back into production.

DE HAVILLAND CANADA Dash 8 Q100

Initial basic model of Dash 8 regional turboprop airliner family.

Followed by the series 100A in 1990 with extra headroom and 100B with more powerful engines.

From 1996 all Dash 8s delivered with a computer controlled noise and vibration suppression system.

Bombardier Aerospace Q400 Dash 8, Canada

Bombardier Aerospace’s Dash 8 family of turboprop regional airliners includes the 37-passenger Q100 and Q200, the 50 to 60-passenger Q300 and the 70 to 80-passenger stretched Q400. The newest member of the Dash 8 family, the Q400, had its first flight in 1998 and entered commercial service in February 2000.

The Q400 Dash 8 airliner was developed by Bombardier to meet the requirements of regional airlines for larger aircraft on high-density, short-haul routes.

De Havilland Aircraft of Canada took over the Q Series aircraft programme from Bombardier in June 2019.

In November 2019, Palma signed a letter of intent with De Havilland Canada to purchase 20 Dash 8-400 aircraft.

TAAG Angola Airlines placed order for six Q400 aircraft in June 2019 and took delivery of the first aircraft in June 2020.

Recent orders for the Q400 NextGen include 20 aircraft from Eurolot in March 2012, five aircraft for Ethiopian Airlines, two for Horizon Air in February 2012, two dual-class Q400 NextGen for RwandAir in February 2014, and ten aircraft for Air Kazakhstan in July 2014.

The aircraft has provision for a flight management system, a global positioning system and a traffic alert and collision avoidance system, TCAS II. Dash 8 Q400 cabin.

Industry-First Extended Service Program PLUS Doubles The Service Life Of The Robust De Havilland Canada Dash 8-100 Aircraft

“Our Extended Service Program, which takes the Dash 8-100 aircraft from 80,000 to 120,000 flight cycles, allows owners and operators alike to derive additional economic benefits from their aircraft, and now our Extended Service Program PLUS, which takes the aircraft to 160,000 flight cycles, provides even more value,” said Robert Mobilio.

“Combined, our two Extended Service Programs add another 30 to 40+ years to the operational life of Dash 8-100 aircraft – that’s double the original service life of the aircraft. This is undeniably an industry first that reinforces De Havilland Canada’s long heritage of building aircraft that stand the test of time and provide exceptional value to owners, operators and the communities that rely on the connectivity they provide.”

An Extended Service Program is also available for the De Havilland Canada Dash 8-300 aircraft.

The original De Havilland Canada Dash 8-100/200/300 aircraft, delivered from 1984 through the mid 1990’s, established themselves as rugged and reliable turboprop aircraft.

The original Dash 8 aircraft has grown into a family of 37- to 90-seat Dash 8 aircraft that offers models – including the technologically advanced Dash 8-400 turboprop – to profitably fit any regional airline mission.

With more than 1,300 aircraft delivered, Dash 8 turboprops continue to provide exceptional operating costs coupled with the benefits of commonality within the Dash 8 family of aircraft.

With more than 5,000 aircraft delivered, De Havilland Aircraft of Canada Limited is well established across the globe and our talented team of aviation professionals is dedicated to advancing our near-100-year reputation for excellence in innovation, production and customer support.

English Language

Although the great influence of these languages on the vocabulary and grammar of Modern English is widely acknowledged, most specialists in language contact do not consider English to be a true mixed language.

The “Inner circle” countries with many native speakers of English share an international standard of written English and jointly influence speech norms for English around the world.

The view of the English language among many Indians has gone from associating it with colonialism to associating it with economic progress, and English continues to be an official language of India.

English is also widely used in media and literature, and the number of English language books published annually in India is the third largest in the world after the US and UK. However, English is rarely spoken as a first language, numbering only around a couple hundred-thousand people, and less than 5% of the population speak fluent English in India.

In a 2012 official Eurobarometer poll, 38 percent of the EU respondents outside the countries where English is an official language said they could speak English well enough to have a conversation in that language.

The influence of English comes from such factors as opinion leaders in other countries knowing the English language, the role of English as a world lingua franca, and the large number of books and films that are translated from English into other languages.

The major native dialects of English are often divided by linguists into the two extremely general categories of British English and North American English.

Origin, History, Development, Characteristics, & Facts

English language, West Germanic language of the Indo-European language family that is closely related to the Frisian, German, and Dutch languages.

English belongs to the Indo-European family of languages and is therefore related to most other languages spoken in Europe and western Asia from Iceland to India.

Though closely related to English, German remains far more conservative than English in its retention of a fairly elaborate system of inflections.

Modern English is analytic, whereas Proto-Indo-European, the ancestral tongue of most of the modern European languages, was synthetic, or inflected.

English is the only European language to employ uninflected adjectives; e.g., the tall man, the tall woman, compared to Spanish el hombre alto and la mujer alta.

As for verbs, if the Modern English word ride is compared with the corresponding words in Old English and Modern German, it will be found that English now has only 5 forms, whereas Old English ridan had 13, and Modern German reiten has 16.

Although a Germanic language in its sounds and grammar, the bulk of English vocabulary is in fact Romance or Classical in origin.

What Is English?

English is a language-originally the language of the people of England.

Today, English is the main language of the United Kingdom, Ireland, the United States of America, Canada, Australia, New Zealand and more than fifty other countries.

English is probably the third language in terms of number of native speakers; and probably the most widely spoken language on the planet taking into account native and non-native speakers.

Consequently English is sometimes described as a “World language” or a “Global lingua franca”.

Small or lowercase formsa b c d e f g h i j k l m n o p q r s t u v w x y z. and capital or uppercase formsA B C D E F G H I J K L M N O P Q R S T U V W X Y Z. English belongs to the West Germanic group of Indo-European languages.

Lingua franca: a language that is used as a common language between people who speak different languages.

Borrow: take a word from another language and use it as your own language.

A Brief History Of The English Language

It must be noted that the English language we know and study through various English language courses today had yet to be created as the inhabitants of Britain spoke various dialect of the Celtic language.

Albert Baugh, a notable English professor at the University of Pennsylvania notes amongst his published works that around 85% of Old English is no longer in use; however, surviving elements form the basis of the Modern English language today.

Late Old English – can be considered the final phase of the Old English language which was brought about by the Norman invasion of England.

It was William Caxton’s innovation of an early printing press that allowed Early Modern English to become mainstream, something we as English learners should be grateful for! The Printing Press was key in standardizing the English language through distribution of the English Bible.

Jamestown, Virginia, also saw the dawn of American English with English colonizers adopting indigenous words, and adding them to the English language.

The idea may have backfired as the English language walked away with a large number of foreign words that have now become part and parcel of the English language e.g. shampoo, candy, cot and many others originated in India!

If one endevours to study various English language courses taught today, we would find almost no immediate similarities between Modern English and Old English.

What Are The Origins Of The English Language?

The history of English is conventionally, if perhaps too neatly, divided into three periods usually called Old English, Middle English, and Modern English.

The following brief sample of Old English prose illustrates several of the significant ways in which change has so transformed English that we must look carefully to find points of resemblance between the language of the tenth century and our own.

It is fiction in the guise of travel literature, and, though it purports to be from the pen of an English knight, it was originally written in French and later translated into Latin and English.

The early part of this period saw the completion of a revolution in the phonology of English that had begun in late Middle English and that effectively redistributed the occurrence of the vowel phonemes to something approximating their present pattern.

Later, as English came into contact with other cultures around the world and distinctive dialects of English developed in the many areas which Britain had colonized, numerous other languages made small but interesting contributions to our word-stock.

Because ancient and modern languages like Old Norse and Gothic or Icelandic and Norwegian have points in common with Old English and Old High German or Dutch and English that they do not share with French or Russian, it is clear that there was an earlier unrecorded language that can be called simply Germanic and that must be reconstructed in the same way.

Still earlier, Germanic was just a dialect of a language conventionally designated Indo-European, and thus English is just one relatively young member of an ancient family of languages whose descendants cover a fair portion of the globe.

Examples Of Minerals, Types, Characteristics & Uses With Videos Of Mineral Resources

What are Mineral Resources? A mineral is a naturally occurring substance, representable by a chemical formula, that is usually solid and inorganic, and has a crystal structure.

Table of Contents Mineral resources are the key material basis for socio-economic development.

Statistical results show that more than 95% of energy used by mankind, 80% industrial raw materials and 70% raw materials for agricultural production are from mineral resources.

Mineral resources can be divided into two major categories.

The total volume of consumable mineral resources is just 1% of all the minerals present in the earth’s crust.

The consumption rate is so high that these mineral resources which are non-renewable will get exhausted very soon.

Frequently Asked Questions – FAQs.What is the importance of mineral resources?What are the uses of minerals?How minerals are found?What defines a mineral?What are the characteristics of minerals?

ScienceDirect Topics

Mineral resources convert to mineral reserves on consideration of ‘Modifying Factors’.

In few specific cases, measured mineral resources convert to probable mineral reserves because of the improbabilities associated with modifying factors without any decrease in the geological knowledge and confidence.

Is the mineral deposit consisting of useful concentration that may or may not exceed economic cost for obtaining the valuable minerals.

The mineral resource becomes mineral or ore reserve.

Reserve is the composite of useful concentration of minerals that may or may not exceed the input cost for obtaining the target valuable minerals.

The mineral/ore deposits are formed in the Earth’s crust by different geological processes over time, and accumulates minerals in such quantities and qualities that it is technologically possible to mine and economically profitable to designate it as “Ore” and “Orebody.” In such condition the mineral resource becomes mineral or ore reserve.

The mineral reserves/resources have been discussed in detail in Chapter 10., Mineral Resource Assessment and Economic Parameters.

Mineral Resources: Definition, Types, Use And Exploitation

Mineral resources are non-renewable and include metals, and non-metals.

Management of mineral resources has to be closely integrated with the overall strategy of development; and exploitation of minerals is to be guided by long-term national goals and perspectives.

Human wealth basically comes from agriculture, manufacturing, and mineral resources.

Our complex modern society is built around the exploitation and use of mineral resources.

Since the future of humanity depends on mineral resources, we must understand that these resources have limits; our known supply of min­erals will be used up early in the third millennium of our calendar.

Further­more, modern agriculture and the ability to feed an overpopulated world is de­pendent on mineral resources to construct the machines that till the soil, enrich it with mineral fertilizers, and to transport the products.

The consumption of natural resources proceeded at a phe­nomenal rate during the past hundred years and population and production increases cannot continue without increasing pollution and depletion of min­eral resources.

Mineral Resources Limited

Mineral Resources is an innovative and leading mining services company with a growing world-class portfolio of mining operations across multiple commodities, including iron ore and lithium.

We have a large footprint providing mining services to clients throughout Western Australia and the Northern Territory, operating mine sites in the Pilbara and Goldfields regions and shipping product through ports in Port Hedland and Esperance.

Mineral Resources Inc.

Founded by Arlo Richardson in 1981, Mineral Resources, Inc. engages in the acquisition of oil and gas leases and the development, production, and sale of oil and natural gas.

We operate in Colorado’s Denver-Julesburg Basin and we take pride in the fact that our team and partners live in the communities where we operate.

MinRes Accelerates Lithium Expansion

Mineral Resources has announced plans to increase production from its Wodgina and Mt Marion mines in response to “Unprecedented global customer demand” for lithium products.

Today’s announcement comes after other producers, notably Pilbara Minerals and Talison Lithium, announced their own expansion plans in WA. It also comes five months after MinRes said it would restart production at Wodgina, which was mothballed in 2019 following a market downturn.

MinRes said today it was well-progressed with its preparations to resume operations at Train 1, with first spodumene concentrate brought forward to May 2022.

MinRes and Albemarle have also agreed to review the market towards the end of this calendar year to assess timing for the start-up of Train 3 and the possible construction of Train 4.

MinRes added that it was still seeking to finalise binding agreements with Albemarle regarding a restructure of their joint venture, which encompasses Wodgina and the Kemerton Lithium Plant.

MinRes said first lithium hydroxide from train 1 at Kemerton was expected by May 2022.

Separately, MinRes said it has agreed with its 50:50 partner Jiangxi Ganfeng Lithium Co to upgrade the processing facilities at their Mt Marion mine.

Mineral Commodity Summaries 2021

Each mineral commodity chapter of the 2021 edition of the U.S. Geological Survey Mineral Commodity Summaries includes information on events, trends, and issues for each mineral commodity as well as discussions and tabular presentations on domestic industry structure, Government programs, tariffs, 5-year salient statistics, and world production and resources.

The MCS is the earliest comprehensive source of 2020 mineral production data for the world.

More than 90 individual minerals and materials are covered by 2-page synopses.

For mineral commodities for which there is a Government stockpile, detailed information concerning the stockpile status is included in the 2-page synopsis.

Reserves and resources information is in Appendix C, which includes “Part A-Resource and Reserve Classification for Minerals” and “Part B-Sources of Reserves Data.” A directory of USGS minerals information country specialists and their responsibilities is in Appendix D. The USGS continually strives to improve the value of its publications to users.

For best results viewing and printing PDF documents, it is recommended that you download the documents to your computer and open them with Adobe Reader.

More information about viewing, downloading, and printing report files can be found here.

Biggest Hard Rock Deposit In The World

The open-pit Wodgina lithium project in the Pilbara region of Western Australia is the biggest hard rock deposit in the world.

MRL is currently expanding the Wodgina project to increase spodumene production and develop an integrated lithium hydroxide operation at the resource site.

MRL entered an agreement with Albemarle Corporation in November 2018 for creating a joint venture with equal share to own and operate the Wodgina lithium mine.

Albemarle has agreed to invest $1.15bn for 50% interest in the JV, which will combine the lithium production and marketing expertise of Albemarle with mining capabilities of MRL. The expansion project will include the installation of a new spodumene concentrate plant and a lithium hydroxide plant, while upgrading the crushing plant.

The first stage is expected to produce 50,000tpa of battery-grade lithium hydroxide, while the remaining spodumene concentrate will be processed and converted into battery-grade lithium hydroxide in the second stage.

As of October 2018, the Cassiterite pit of Wodgina lithium mine was estimated to hold 151.9Mt of probable ore reserves grading 1.17% lithium.

Hatch conducted the pre-feasibility study of the hydroxide plant at Wodgina, in addition to feasibility study of the proposed downstream plant to produce lithium hydroxide or lithium carbonate.

Major Mines & Projects

The Wodgina pegmatite district contains a number of prospective pegmatite groups, including the Wodgina Deposit.

The Wodgina lithium mineralisation is hosted within a number of sub-parallel, sub-horizontal, northeast trending pegmatite intrusive bodies which base of the massive pegmatite apparently with a dip at between 5° to 30° to the west-southwest.

The massive basal pegmatite varies from 120m to 200m thick.

The lithium in the Cassiterite Pit and shallower pegmatites occurs as 10 – 30 cm long grey-white spodumene crystals within medium grained pegmatites comprising primarily of quartz, feldspar, spodumene and muscovite.

Typically the spodumene crystals are oriented orthogonal to the pegmatite contacts.

Some zoning of the pegmatites parallel to the contacts is observed, with higher concentrations of spodumene occurring close to the upper contact.

In the massive basal pegmatite, the spodumene is distributed within fine-grained quartz, feldspar, spodumene and muscovite matrix.

Albemarle, Mineral Resources To Speed Up Wodgina Restart

Mineral Resources and Albemarle, the world’s no.1 lithium producer, also agreed to accelerate a restart of Train 2, from which first production is expected in July.

Each train has a nameplate capacity of 250,000 tonnes, Mineral Resources said in the statement.

The companies, which have been working together in the Wodgina mine and the Kemerton lithium hydroxide conversion trains in the Pilbara region of Western Australia since 2019, also will assess timing to start on Train 3 and a possible construction of Train 4.

Operations at the Wodgina mine were halted in late 2019 because of then-weak markets, but the companies have been working to resume production at the site in recent months.

Albemarle is also a joint venture partner to China’s Tianqi Lithium to develop the Greenbushes mine and processing plant in Western Australia.

Mineral Resources also announced that is upgrading the processing facilities at its Mt Marion hard rock lithium mine, a 50-50 joint venture with China’s Jiangxi Ganfeng Lithium.

Located 40km south-west of Kalgoorlie, in the Goldfields region of Western Australia, Mount Marion contains the world’s second biggest high-grade lithium concentrate reserves.

Albemarle, Mineral Resources To Speed Up Wodgina Lithium Mine Restart

Albemarle and its partner Mineral Resources will speed up the restart of production at their jointly owned Wodgina lithium mine in Australia to respond to “Unprecedented” demand for the battery metal.

Mineral Resources and Albemarle, the world’s no.1 lithium producer, also agreed to accelerate a restart of Train 2, from which first production is expected in July.Each train has a nameplate capacity of 250,000 tonnes, Mineral Resources said in the statement.

The companies, which have been working together in the Wodgina mine and the Kemerton lithium hydroxide conversion trains in the Pilbara region of Western Australia since 2019, also will assess timing to start on Train 3 and a possible construction of Train 4.A decision on the matter will be based on global lithium market conditions later this year, they said.

Operations at the Wodgina mine were halted in late 2019 because of then-weak markets, but the companies have been working to resume production at the site in recent months.

Albemarle is also a joint venture partner to China’s Tianqi Lithium to develop the Greenbushes mine and processing plant in Western Australia.

Mount MarionMineral Resources also announced that is upgrading the processing facilities at its Mt Marion hard rock lithium mine, a 50-50 joint venture with China’s Jiangxi Ganfeng Lithium.

Located 40km south-west of Kalgoorlie, in the Goldfields region of Western Australia, Mount Marion contains the world’s second biggest high-grade lithium concentrate reserves.

Mineral Resources Responds To Global Lithium Demand

Mineral Resources will increase production from its Wodgina and Mt Marion spodumene mines in Western Australia in response to unprecedented global customer demand for lithium products.

MRL managing director Chris Ellison said that the growing demand for lithium has been driven by the strength of the electric vehicle market.

“This demand has resulted in a substantial increase in lithium prices, with pricing expected to remain strong for the rest of this decade,” he said.

Alongside Albemarle, MRL decided to accelerate the resumption of production from Train 2 at Wodgina, with the first spodumene concentrate expected in July 2022.

MRL and Albemarle agreed to review the state of global lithium market toward the end of this calendar year, to reassess the timing for the start-up of Train 3 and the possible construction of Train 4.

MRL and its 50/50 joint venture partner Jiangxi Ganfeng Lithium agreed to upgrade the Mt Marion procession facilities, given the positive metallurgical test work results and the completion of project studies at the mine.

“With a world-class portfolio of highest-quality, long-life lithium assets in a Tier 1 mining jurisdiction, we are well-positioned to capitalise on the continued growth of the global electric vehicle market.”

Monsters Of Rock: MinRes Wants To Expand Lithium Production As Spodumene Edges Towards US$6000/T

MinRes shares soar after announcing major expansions of Wodgina and Mt Marion lithium JVs. Spodumene spot sales in the China market averaging US$5750/t: Fastmarkets.

Prices for spodumene, the 6% lithium concentrate produced by hard rock miners in Australia for sale to Asian battery makers, have held over US$5000/t on the spot market over the course of the last month.

That’s somewhere around 11 to 12 times the cost of production in WA, inflation not withstanding, encouraging MinRes and its partners to go full throttle.

“MinRes and Albemarle have also agreed to review the state of global lithium market towards the end of this calendar year to assess timing for the start-up of Train 3 and the possible construction of Train 4,” MinRes said, a ramp up that would make Wodgina a million tonne a year operation.

The first train of the Kemerton lithium hydroxide plant MinRes is building with Albemarle in a 40-60 partnership is expected to produce its first battery grade chemicals in May after spodumene feed was introduced recently, with a second train targeting mechanical completion and first product in the December quarter.

The companies are already looking at the development of further processing capacity for their Wodgina mine as well, with all spodumene ultimately to be processed through conversion facilities either built or acquired by a new 50-50 JV between MinRes and Albemarle.

“For some time now the world has seen extraordinary demand for lithium, driven by the strength of the electric vehicle market. This demand has resulted in a substantial increase in lithium prices, with pricing expected to remain strong for the rest of this decade,” MinRes MD Ellison said.

Albemarle, Mineral Resources To Speed Up Wodgina Lithium Mine Restart – Market Trading Essentials

Mineral Resources and Albemarle, the world no.1 lithium producer, also agreed to accelerate a restart of Train 2, from which first production is expected in July.

Each train has a nameplate capacity of 250,000 tonnes, Mineral Resources said in the statement.

The companies, which have been working together in the Wodgina mine and the Kemerton lithium hydroxide conversion trains in the Pilbara region of Western Australia since 2019, also will assess timing to start on Train 3 and a possible construction of Train 4.

A decision on the matter will be based on global lithium market conditions later this year, they said.

Operations at the Wodgina mine were halted in late 2019 because of then-weak markets, but the companies have been working to resume production at the site in recent months.

Albemarle is also a joint venture partner to China’s Tianqi Lithium to develop the Greenbushes mine and processing plant in Western Australia.

Mineral Resources also announced that is upgrading the processing facilities at its Mt Marion hard rock lithium mine, a 50-50 joint venture with China’s Jiangxi Ganfeng Lithium.

Innocent Drinks

Innocent Drinks is a company that produces smoothies and juice sold in supermarkets, coffee shops and various other outlets.

Revenue for the company declined in 2009 as a result of the global financial crisis which led to an overall loss of £8.6m. On 6 April 2009, Innocent Drinks announced on its website an agreement to sell a stake of 10-20% to The Coca-Cola Company for £30 million, with the three founders continuing to retain operational control.

An Innocent smoothie consists of whole crushed fruit and juices, but other ingredients such as carrots and ginger have been used in some drinks.

Innocent Drinks discovered that one of their supplies was contributing to the unsustainable water use threatening UNESCO World Heritage site Doñana National Park, one of Europe’s most important wetlands.

In 2022, the Advertising Standards Authority banned an Innocent drinks ad that claimed the company’s products have a positive enironmental impact.

In October 2007 Innocent was warned by the Advertising Standards Authority for making unsubstantiated claims about the health benefits of their “Superfoods” smoothies, stating that their marketing claims could not be backed up by medical science and ordering Innocent not to repeat them.

The Innocent Foundation is a registered charity funded by the employees, shareholders and company of Innocent drinks.

Brand Purpose And Responsibility

Everyone’s favourite healthy drinks vendor, social media and brand marketing gurus.

You’d be hard up to find a brand that resonates better than these smooth-talking smoothie makers.

Brand responsibility is often chalked up to what a brand does for factors such as sustainability, whether they give to charity, donate to the NHS, support important societal movements etc.

While Innocent DO do all of those things, their brand responsibility and stature isn’t limited to that.

They’ve done such an amazing job in building it, the foundations are pretty much set in stone, and this stance is sure to only strengthen their brand.

It also further demonstrates their care and brand responsibility to take a side on important current affairs.

Innocent’s brand responsibility lies solely in being ‘one of the good guys’.

Innocent Drinks Ads Banned Over Environmental Claim

Adverts for drinks firm Innocent have been banned after the advertising regulator ruled they “Misled” customers over the firm’s environmental impact.

The watchdog said the adverts did not show that Innocent’s single-use plastic products had a “Net positive” environmental impact over their full life cycles.

Twenty-six viewers, one of whom identified themselves as representing environmental group Plastics Rebellion, complained to the Advertising Standards Authority that the adverts misled customers by exaggerating the “Total environmental benefits” of the drinks.

The regulator said that because the ads “Implied that purchasing Innocent products was a choice which would have a positive environmental impact when that was not the case”, it concluded that the ads were “Misleading.”

In the ruling, Innocent responded that there was no suggestion in the ads that buying Innocent products would lead to a positive environmental impact.

Mother advertising agency declined to comment when approached by the BBC. In a statement, Plastics Rebellion said that Innocent were being “Disingenuous” about the dangers of plastic’s threat to human health and environment, as well as “Trivialising the horrific scale of the problem by repeating the mantra: ‘Reduce, re-use, recycle'”.

The watchdog also banned an Aqua Pura advert earlier this year for the claim “100% recycled bottle” because not all of the parts of the bottle were recycled and warned the firm to ensure they did not “Overstate the environmental benefit” of their brand and products, and did not claim that products made of plastic were “Eco-friendly” or “Nature friendly”.

Adverts for drinks firm Innocent have been banned after the advertising regulator ruled they “Misled” customers over the firm’s environmental impact.

The regulator said it implied buying Innocent drinks “Was a choice which would have a positive environmental impact when that was not the case”,.

The Advertising Standards Authority said the adverts did not show that Innocent’s single-use plastic products had a “Net positive” environmental impact over their full life cycles.

In the ruling, Innocent responded that there was no suggestion in the ads that buying Innocent products would lead to a positive environmental impact.

Innocent said: “Our advert was always intended to highlight important global environmental issues and the need for collective action to make a change. We transparently share more about the work that we do on sustainability on our website.”As with any new guidelines, we’d like to work with the ASA and other brands to understand how to align to them to continue the conversation on these important topics.

Mother advertising agency declined to comment when approached by the BBC.In a statement, Plastics Rebellion said that Innocent were being “disingenuous” about the dangers of plastic’s threat to human health and environment, as well as “trivialising the horrific scale of the problem by repeating the mantra: ‘Reduce, re-use, recycle'”.

Coca-Cola, owner of Innocent, produces about three million tonnes of plastic packaging a year – equivalent to 200,000 bottles a minute.

Marketing Strategy Of Innocent Drinks, Sample Of Business Plans

Innocent drinks has a long range of products which they claim to be made up of pure and fresh fruit and which are free from any kind of preservatives.

Innocent made their brand stand out from the crowd by adopting innovative ways of marketing and that was their beginning in differentiating their product from their competitors Brand name is very critical and it should be consistent with what the company is trying to deliver and how it wants to be perceived by customers.

Innocent drinks is enjoying product width from smoothies to veg.

Innocent has used different approach for its marketing by targeting consumers of different products with different advertisements and campaigns.

In the beginning, Innocent used the local shop for its products but as the popularity of products multiplied, the company gradually gained a great market share.

Innocent drinks use intensive distribution strategy by placing their product in as many places and outlet as possible.

As the market is becoming more global, there will always arise new opportunities but also threats as consumers also have access to variety of products from different countries with different tastes and nutritional values so innocent drinks must consider what their consumers want, their preferences if they want to survive and be successful in the long term.

Innocent Smoothies Brand: Marketing Communication

With the re-positioning of the Innocent brand in the United Kingdom Market, Innocent Company aims at changing the consumption patterns among its target group of 18-34 years old.

Just like Innocent Company, there also exist numerous companies that supply the market with soft drinks and smoothies.

The increasing retail power and brand competition has triggered the need for the company to adopt IMC. Worldly, competition is increasingly becoming more fierce as brand new products gets into the principal markets and the traditional and existing producers improves on product quality, viticulture practices and of great significance, brand communication and marketing skills.

The model helps in the interpretation and analysis of how consumers perceive a company’s product or service as self-reliant and how it impacts on their daily lives such as the Innocent smoothies which improves their life as it is healthy and made form natural products rather than food concentrates.

Innocent smoothies are a company that can make maximum use of its marketing strategies without necessarily interfering with the cost of the products.

The smoothies brand of the Innocent Company is quite unique.

Integrated marketing communication will help innocent company in informing, persuading and reminding the company’s target customers about the services and products unique benefits available in the market.

Innocent

WOW, NICE SHOT Said 100% of the people we asked who drank one of our juice shots.

WOW, WHAT A SHOT Said 0% of the people we asked to rate our Marcus’ shooting technique in this video.

10 people we asked who were sat around us when we posted this ** the same 10 people + also Marcus when we asked him if he was proud of what he did.

Coffea Arabica

Arabica coffee originates from Ethiopia and was first cultivated in Yemen, and documented by the 12th century.

The conservation of the genetic variation of C. arabica relies on conserving healthy populations of wild coffee in the Afromontane rainforests of Yemen.

Arabica coffee production in Indonesia began in 1699 through the spread of Yemen’s trade.

Coffea arabica accounts for 60% of the world’s coffee production.

Gourmet coffees are almost exclusively high-quality mild varieties of arabica coffee, and among the best known arabica coffee beans in the world are those from Jamaican Blue Mountain, Colombian Supremo, Tarrazú, Costa Rica, Guatemalan Antigua, and Ethiopian Sidamo.

While beans of normal C. arabica plants contain 12 mg of caffeine per gram of dry mass, these mutants contain only 0.76 mg of caffeine per gram, but with taste similar to normal coffee.

The more heat-tolerant Coffea stenophylla may replace C. arabica as the dominant coffee species in cultivation in order to guard against this.

ScienceDirect Topics

Coffee consumption has shown beneficial effect in different kinds of liver diseases like cirrhosis, HBV and HCV infections, and HCC. Coffee extract and its constituents have shown inhibitory effect on HBV replication in HepG2.

Despite coffee consumption being sometimes associated with increases in cardiovascular disease risk factors, including high blood pressure and plasma homocysteine levels, most evidence suggests that a regular intake of caffeinated coffee does not increase the risk of hypertension and other cardiovascular diseases.

Biogeography of Coffee Coccid PestsThere are three economically important species of coffee: Coffea arabica.

Arabica coffee accounts for 80% of world trade and robusta coffee for most of the remaining 20%. Although Coffea species are native to Africa, commercial plantations of arabica and/or robusta coffee are now grown in many tropical countries around the world.

The concentration of sucrose in green coffee is usually lower in robusta and higher in arabica varieties, while the concentration of free asparagine in robusta coffees is normally higher than in arabica ones.9 Nevertheless, this may vary significantly due to cultivation practices and processing.

The main distinction between the chemical composition of washed and natural coffee is the soluble solids content, which is higher in the case of natural coffee.

The quantity of acrylamide in roasted coffee is usually higher in robusta than in arabica coffees but, regarding the precursors, a weak correlation between acrylamide and asparagine was observed, and no correlation with reducing sugars was found.

Coffea Arabica

Cup expresso coffee 310 mg Cup boiled coffee 100 mg Cup instant coffee 65 mg Cup tea 10-50 mg Cup cocoa 13 mg Can cola 25 mg Can coca cola 20 mg Cup mate 25-50 mg Can pepsi cola 10 mg Tablet Caffeine 100-200 mg Tablet(800 mg) Zoom 60 mg In humans, caffeine, 1,3,7-trimethylxanthine, is demethylated into three primary metabolites: theophylline, theobromine, and paraxanthine.

Inhalation of coffee bean dust can produce coffee worker’s lung, a type of allergic alveolitis.

C. arabica is only natural tetraploid and completely self-fertile coffee.

Arabica coffee thrives from the humid tropics to temperate climates from 5°N lat.

Arabica coffee makes up 90% of the world’s coffee; world production being about 70.7 million bags of 60 kg each.

Coffee hulls contain 3,885, and dry robusta coffee contains3,915 calories.

If legume shade trees are interplanted with the coffee, we expect more firewood from the intercrop and less from the coffee.

Coffea Arabica

Plants prefer climates with daytime temperatures of 70-80°F and nighttime temperatures of 60-65°F. Leaf drop may occur when temperatures dip below 55°F. Plants may be grown indoors in containers with a fast-draining potting soil.

Indoor plants like bright sunny windows, but when taken outdoors appreciate light shade.

Coffea arabica, commonly called Arabian coffee, is an upright tropical evergreen shrub or small tree that grows to 10-15′ tall.

In coffee plantations, plants are kept trimmed to 6′ tall for ease of harvest and best production.

Indoor container plants typically grow to about 4-6′ tall.

Plants feature glabrous, glossy, elliptical, dark green leaves with prominent veins and wavy margins, fragrant, star-shaped, white flowers that bloom in axillary clusters of 2-9, green two-seeded fruits that gradually mature to yellow, light red and finally deep red and fissured bark on older branches.

Elsewhere, it makes an attractive container plant for sun rooms that can be taken outside to patio areas in summer.

How To Grow Coffe Arabica Indoors

The coffee plant coffea arabica is a rather rare sight inside your own place.

Homegrown coffee can only be harvested, if one manages to get the plant to blossom and the red coffee cherries to develop.

Coffee plants are poured plentily from spring to autumn, young plants need more water than older ones.

On the common market you only find plants of the variety coffea arabica ‘nana’.

The plant is self- pollinating so there is no need for a second plant.

If you do not want to grow the plant yourself, you can purchase them in store.

You should remember that coffee plants grow very bushy and sweeping and can reach heights of up to 150 centimeters.

FPS135/FP135: Coffea Arabica Coffee

Each berry contains two seeds or coffee beans suitable for home roasting and grinding.

Reaching a height of 15 feet, coffee tree is a great conversation piece, growing in light rich soil and partial shade.

Regular pruning can keep the plant attractive at any desirable size.

This handsome shrub is suitable for containers, specimen plantings, or used as a small understory tree in hammocks and wild wooded areas.

Coffee plants are bothered by scales, mites, thrips, caterpillars, and mineral deficiencies.

What Is Coffee?

Everyone recognizes a roasted coffee bean, but you might not recognize an actual coffee plant.

The average coffee tree produces 10 pounds of coffee cherry per year, or 2 pounds of green beans.

All commercially grown coffee is from a region of the world called the Coffee Belt.

In the commercial coffee industry, there are two important coffee species – Arabica and Robusta.

Coffea Arabica is descended from the original coffee trees discovered in Ethiopia.

These trees produce a fine, mild, aromatic coffee and represent approximately 70% of the world’s coffee production.

The Anatomy of a Coffee Cherry The beans you brew are actually the processed and roasted seeds from a fruit, which is called a coffee cherry.

Anatomy, Blood Vessels

The peripheral vascular system includes all the blood vessels that exist outside the heart.

The presence of elastin in the large blood vessels enables these vessels to increase in size and alter their diameter.

As the diameter of the blood vessels decreases, the velocity of blood flow also diminishes.

Angiogenesis is the process in which new blood vessels derive from the endothelial layer of a pre-existing vessel.

The walls of large blood vessels, like the aorta and the vena cava, are supplied with blood by vasa vasorum.

Although vessels only contain smooth muscles, the contraction of skeletal muscle plays an important role in the movement of blood from the periphery towards the heart in the venous system.

6.Sheng Y, Zhu L. The crosstalk between autonomic nervous system and blood vessels.

Blood Vessels: Types, Anatomy, Function & Conditions

It regulates blood pressure, prevents blood clots and keeps toxins out of your blood.

Conditions and Disorders What conditions and disorders affect the blood vessels?

Blood vessel walls can thicken and narrow, which prevents blood from flowing freely.

Medication: Some people need medication to manage their blood pressure, reduce their risk of blood clots or lower their cholesterol levels.

Interventional procedures can treat blood clots, aneurysms and severely narrowed blood vessels.

Surgery: You may need open surgery for some blood vessel conditions that don’t improve with medication or other nonsurgical treatments.

Blood vessels carry blood from your heart to the rest of your body.

Anatomy, Blood Vessels

The peripheral vascular system includes all the blood vessels that exist outside the heart.

Arteries play a major role in nourishing organs with blood and nutrients.

The presence of elastin in the large blood vessels enables these vessels to increase in size and alter their diameter.

As the diameter of the blood vessels decreases, the velocity of blood flow also diminishes.

The venous system can accommodate a large volume of blood at relatively low pressures, a feature termed high capacitance.

At any point in time, nearly three-fourths of the circulating blood volume is contained in the venous system.

The forward blood flow from the lower extremities to the heart is also influenced by respiratory changes that affect pressure gradients in the abdomen and chest cavity.

Blood Vessel

There are five types of blood vessels: the arteries, which carry the blood away from the heart; the arterioles; the capillaries, where the exchange of water and chemicals between the blood and the tissues occurs; the venules; and the veins, which carry blood from the capillaries back towards the heart.

The term “Arterial blood” is nevertheless used to indicate blood high in oxygen, although the pulmonary artery carries “Venous blood” and blood flowing in the pulmonary vein is rich in oxygen.

Blood vessels also circulate blood throughout the circulatory system Oxygen is the most critical nutrient carried by the blood.

Resistance is an accumulation of three different factors: blood viscosity, blood vessel length, and vessel radius.

Blood viscosity is the thickness of the blood and its resistance to flow as a result of the different components of the blood.

In contrast, occlusion of the blood vessel by atherosclerotic plaque, by an embolised blood clot or a foreign body leads to downstream ischemia and possibly infarction.

Vessel occlusion tends to be a positive feedback system; an occluded vessel creates eddies in the normally laminar flow or plug flow blood currents.

The Franklin Institute

Blood vessels may be tiny but they cover a lot of ground.

The smallest blood vessels measure only five micrometers.

There are three kinds of blood vessels: arteries, veins, and capillaries.

Arteries carry oxygenated blood away from the heart.

The arteries deliver the oxygen-rich blood to the capillaries, where the actual exchange of oxygen and carbon dioxide occurs.

The capillaries then deliver the waste-rich blood to the veins for transport back to the lungs and heart.

Unlike arteries, veins contain valves that ensure blood flows in only one direction.

Definition, Anatomy, Function, & Types

Blood vessel, a vessel in the human or animal body in which blood circulates.

Very small branches that collect the blood from the various organs and parts are called venules, and they unite to form veins, which return the blood to the heart.

Capillaries are minute thin-walled vessels that connect the arterioles and venules; it is through the capillaries that nutrients and wastes are exchanged between the blood and body tissues.

The inner surface of every blood vessel is lined by a thin layer of cells known as the endothelium.

The endothelium plays a critical role in controlling the passage of substances, including nutrients and waste products, to and from the blood.

Under certain circumstances, tissues may grow new blood vessels, a process known as angiogenesis.

In humans, the function and structure of blood vessels can be affected by a number of different diseases and conditions.

Blood Vessel Disease: Symptoms, Risk Factors, Types & Treatment

Blood vessel disease is also known as peripheral vascular disease or we can call it artery disease.

The blood vessel disease is a condition of narrowing of the veins and arteries that carry blood to and from the arms, abdomen, and legs.

People over the age of 50 or who have a family history of heart or blood vessel diseases are at higher risk of developing the blood vessel disease.

A person may at higher risk for blood vessel disease if he/she;.

The most common type of blood vessel disease are high blood pressure, or hypertension, and is caused due to the increased pressure of the blood moving through the vessels.

As it is already defined that the disease blocked or narrowed the blood vessels so ultimately the disease is so small, so surgery is usually not a treatment option for it.

As the blood vessel disease can be slowed or prevented with the better and healthy lifestyle choices like exercising every day, eating a low fat and high in fiber diet, visiting the doctor regularly, managing the stress levels, having blood pressure checked, and quitting smoking.

Overview, How It Works, Environmental Impact

Fast fashion is an expression used to refer to the growing popularity of rapidly produced and consumed fashion created to meet fast-changing trends.

Fast fashion gives consumers the ability to stay on top of the current fashions in a somewhat affordable way.

Many believe there must be a considerable shift in how many leading retailers operate to mitigate the negative effects that fast fashion is creating.

Consumers can choose to decrease the adverse effects of fast fashion.

At the end of the day, it all comes down to consumers putting in the effort to care about the harmful effects of fast fashion and make a conscious effort to change that.

Fast fashion refers to the rapidly developed, marketed, and produced lines of clothing created to follow the fashion trends of our world.

Tied to the economic successes, there have also been massive environmental impacts associated with fast fashion.

What Is Fast Fashion And Why Is It A Problem?

Fast fashion is ‘fast’ in a number of senses: the changes in fashion are fast, the rate of production is fast; the customer’s decision to purchase is fast; delivery is fast; and garments are worn fast – usually only a few times before being discarded.

At the time of writing, fast fashion brand Shein featured 21,139 clothes under the ‘New in’ section of its website.

In the BBC’s ‘Breaking Fashion’ show we see Manchester-based fast fashion company, In the Style, reproducing a bodysuit worn by Kylie Jenner.

The exploitation of workers in fast fashion supply chains is partly the result of brands pressuring suppliers to produce clothes as cheaply and quickly as possible.

The low-cost of fast fashion items encourages fast sale.

The problems with fast fashion What are the environmental problems with fast fashion?

Across four major online fast fashion brands, the use of recycled fabrics was a mere 4%. Our analysis of Shein’s website found its recycled content was even lower, at only 0.5%, despite the brand claiming, “When selecting materials, we do our best to source recycled fabric, such as recycled polyester.”

The Chinese fast-fashion retailer Shein has been valued at $100 billion in a new fundraising, more than the combined market capitalisations of Inditex and H&M, the two biggest clothing companies in the world.

Shein has secured the valuation after raising between $1 billion and $2 billion from investors including General Atlantic, Tiger Global Management and Sequoia Capital China.

The valuation beats its mooted $15 billion value in 2020 and is well ahead of Zara owner Inditex’s $68 billion and H&M’s $20 billion, retailers which have thousands of stores globally.

The fundraising was first reported by The Wall Street Journal.

Shein grew from an online wedding dress seller into a clothing powerhouse producing 6,000 new items a day and shipping to.

Fast Fashion Startup Shein Valued At $100B-More Than ZARA, HM Combined

Shein, the Gen Z-favorite online apparel retailer, is now worth as much as General Electric and more than Zara and H&M combined.

Shein recently raised a round of funding at a private-market valuation of $100 billion, Bloomberg and The Wall Street Journal reported April 4, a figure unheard of among fashion companies.

Shein’s publicly traded rivals, Zara and H&M, are valued far less.

Shein takes the fast fashion model to the next level.

Shein follows the tried-and-true fast fashion rule of churning out endless off-the-runway styles at rock bottom prices, but takes it to the next level.

Most of them are priced between $8 and $30. That’s 30 percent to 50 percent less than comparable pieces sold by Zara and H&M. Thanks for its entirely digital sales model, Shein saw its popularity soar during the pandemic as more people turned to online shopping.

In May 2021, Shein overtook Amazon as the most downloaded shopping app in the U.S. Analysts believe Shein’s revenue is on track to surpass that of Inditex this year.

Can We Break The Cycle Of Fast Fashion?

“I only shop fast fashion because I feel I have no other choice,” Stevie Minacs tells me over Zoom.

Fast fashion, typically defined as cheap, trendy clothing meant for short-term wear, has been a foundation of globalized living since the late 1990s, when textile manufacturing became easier thanks to sweatshops in the developing world and efficient supply chains.

Two years into a global pandemic that has threatened incomes and access to differentiated shopping experiences, fast fashion has further tightened its grip.

“Before fast fashion, people just owned fewer garments,” says Kelly Drennan, founding executive director of Fashion Takes Action, the Canadian sustainability-focused non-profit behind the World Ethical Apparel Roundtable educational webinar series.

The threat fast fashion poses is nothing new, and there is increased pressure being put on governments to force brands to comply with what climate activists see as essential measures by imposing tariffs on imported goods that do not meet sustainability standards and incentivizing upcycling.

“The model of fast fashion is not sustainable, but it’s not going anywhere, so I think that these brands have a responsibility to take leadership positions in this area or at the very least follow what other innovative brands are doing,” she says.

The post Can We Break the Cycle of Fast Fashion? appeared first on Elle Canada.

EU Proposes Rules That Discourage Fast Fashion Culture: ‘Longer-Lasting Products’

The European Union is looking to discourage fast fashion culture in its member countries.

The proposed rules are packaged in the commission’s EU Green Deal.

If passed, the rules would set up a “Sustainable and circular textile” action plan that would mandate recycled fiber quotas, eco-friendly designs and digital product passports for repair and reuse tracking.

These proposed rules would aim to get clothing companies in the EU on board by 2030, according to the commission’s press release on the topic.

LULULEMON ENTERS FOOTWEAR BUSINESS WITH 4-PIECE COLLECTION. Statistics compiled by the commission’s EU Data Crunch team found that 9,000 liters of water are used to produce the textiles a European consumer typically buys in a single year.

The Oxford Dictionary defines fast fashion as “Inexpensive clothing produced rapidly by mass-market retailers in response to the latest trends.”

Attitudes about disposable clothing have shifted in recent years as consumers and brands acknowledge the effects fast fashion and textile waste have had on climate change.

What Is Fast Fashion And Why Is It So Bad?

What is fast fashion? Why is fast fashion so bad? And how exactly does it impact people, the planet, and animals?

Fast fashion’s negative impact includes its use of cheap, toxic textile dyes-making the fashion industry the one of the largest polluters of clean water globally, right up there with agriculture.

Fast fashion makes us believe we need to shop more and more to stay on top of trends, creating a constant sense of need and ultimate dissatisfaction.

As an increasing number of consumers call out the true cost of the fashion industry, and especially fast fashion, we’ve seen a growing number of retailers introduce so-called sustainable and ethical fashion initiatives such as in-store recycling schemes.

The anniversary of the Rana Plaza collapse is now Fashion Revolution Week., where people all over the world ask questions like, “Who made my clothes?” and “What’s in my clothes?” Fashion Revolution declares that “We don’t want our clothes to exploit people or destroy our planet”.

Ultra fast fashion brands like SHEIN are selling more than ever, and these young shoppers are their target market.

Learn about fast fashion’s sustainable alternative, slow fashion.

Vasant Narasimhan

Since becoming CEO of Novartis in 2018, Vas has led a strategic and cultural transformation to build a focused medicines company powered by technology leadership in R&D, data science, word-class commercialization and global access to medicine.

Vas has focused his education and career on improving human health and on his personal purpose of inspiring a healthier world.

He continues to champion access and global health priorities, including through a commitment by Novartis to expand access to innovative medicines in low- and middle-income countries by at least 200% by 2025.

At Novartis, we are reimagining medicine by using innovative science and technology to address some of society’s most challenging and long-standing healthcare issues.

Since joining Novartis in 2005, Vas has held a range of leadership roles, including Global Head of Development for Novartis Vaccines, and Global Head of Drug Development and Chief Medical Officer.

In recognition of his sustained efforts to improve human health, he is an elected member of the National Academy of Medicine in the US. As CEO, Vas is transforming Novartis to unleash the creativity of employees and make culture a driver of innovation, reputation and performance.

Vas has also sparked a digital revolution at Novartis; the company is using data science and digital technology to find new ways to discover and develop medicines and increase efficiency.

Vasant Narasimhan

Vasant “Vas” Narasimhan is an Indian-American physician and the chief executive officer of Novartis.

Narasimhan received his bachelor’s degree in biological sciences from University of Chicago, his M.D. from Harvard Medical School and his master’s degree in public policy from the John F. Kennedy School of Government.

Narasimhan has previously served as Global Head of Biopharmaceuticals & Oncology Injectables at Sandoz International.

In 2015, Fortune listed Narasimhan 7th in their ’40 under 40′ list.

Narasimhan married Srishti Gupta in 2003, after meeting her at Harvard while organizing an Asian cultural festival.

Narasimhan’s mother is a former nuclear engineer for Public Service Electric and Gas and his father was an executive at Hoeganaes Corporation.

Narasimhan is a vegetarian and lives in Basel, Switzerland, with his wife and two sons.

Vasant Narasimhan, M.D.

Since becoming CEO, Dr. Narasimhan has led a strategic and cultural transformation at Novartis to build a leading medicines company globally powered by advanced therapy platforms and data science.

Under his leadership, the company has completed over USD 70 billion in strategic transactions.

Prior to that, he held a range of leadership roles in product development and general management, such as Global Head of Development for Novartis Pharmaceuticals from 2014 to 2016; Global Head of the Sandoz Biopharmaceuticals and Oncology Injectables business unit in 2014; Global Head of Development for Novartis Vaccines from 2012 to 2014; and North America Region Head for Novartis Vaccines, as well as United States Country President for Novartis Vaccines and Diagnostics, from 2008 to 2012.

During his career at Novartis, Dr. Narasimhan has overseen the licensure of over 30 novel medicines, including cell and gene therapies and vaccines.

Dr. Narasimhan received his doctor of medicine from Harvard Medical School, a master’s degree in public policy from Harvard’s John F. Kennedy School of Government, and a bachelor’s degree in biological sciences from the University of Chicago in the U.S. During and after his medical studies, he worked extensively on a range of public health issues in low- and middle-income countries, and he continues to champion global health priorities today.

Dr. Narasimhan is a member of the National Academy of Medicine and sits on the board of fellows of Harvard Medical School.

He also serves on the boards of African Parks, a nonprofit conservation organization, and of the Pharmaceutical Research and Manufacturers of America.

Facts, Childhood, Family Life & Achievements Of CEO Of Novartis.

His father, Dr. Kalathur Narasimhan, had once served as the vice president for research and development at the Hoeganaes Corporation while his mother, Gita Narasimhan, is a former nuclear engineer for Public Service Electric & Gas, and a lecturer in physics at Burlington County Community College.

In 2013, Narasimhan was promoted to the position of Global Head, Development.

As the first ever Chief Medical Officer of Novartis, he has the major responsibility of aligning the functions of the various departments within the Novartis Development organization under a unified, global umbrella.

He is a member of the Executive Committee of Novartis as well.

His responsibilities in this position include overseeing the working of all Novartis Group companies and leading a team of over 15,000 employees across 140 global Development programs.

He became a member of the Board of Trustees of the Novartis Foundation in January 2017.

Although Vas Narasimhan is only in his early 40s, he is a much accomplished leader at Novartis.

Novartis CEO Vasant Narasimhan Sees Consistent Growth While Sitting On Cash

The Novartis CEO is sitting on a $20.7 billion war chest, won when the Swiss company sold its stake in Roche Holding this fall.

Novartis , with a market value of nearly $180 billion, is among the largest biopharma firms in the world, but its stock has been left behind over the past 12 months as shares of peers like Pfizer and Eli Lilly have soared.

Novartis ADRs have eked out a gain of 5.9% over the past three years, while the S&P 500 Pharmaceuticals index is up 25.9%, and the S&P 500 index has risen 78.5%. Novartis has so far missed out on the Covid-19 vaccines and therapeutics frenzy, which pushed up investor interest in its peers, and on this year’s excitement over Alzheimer’s disease therapeutic approvals, which pushed up shares of other peers.

“Novartis is built to be a consistent growth story,” Narasimhan says.

Novartis expects to grow sales more than 4% per year on a compounded annualized basis through 2026, and says it has up to 20 assets with billion-dollar-plus sales potential that could be approved over the next five years.

Narasimhan now says Novartis is considering the future of Sandoz, a division specializing in generic drugs.

Narasimhan sees “The full range of options” for what to do with Sandoz.

Vas, a US citizen, had been with the Swiss firm for 12 years, and while he was global head of drug development, he was still a long way down the pecking order.

While you might think that putting someone relatively young in charge of a global firm is a bit unusual – Vas’ life story makes things become a lot clearer.

Born in Pittsburgh in 1976, to parents who had emigrated to the US from India, Vas had the benefit of a pretty good scientific background – his dad was a chemist, and his mother was a nuclear scientist.

After getting his doctorate in medicine from Harvard in 2003, Vas says he thought of practicing medicine, but instead joined the World Health Organisation, where he spent a year working on its efforts to boost public health around the globe.

Barbara Obstoj-Cardwell, editor of The Pharma Letter, a website providing news and analysis on the pharmaceutical sector, says that Vas has a “charismatic presence”.

“Vas Narasimhan appears to have brought plenty of energy, dynamism and ambition since taking over at Novartis – and so far, the results have largely been impressive.

Based at the firm’s head office in Basel, there has never been a language barrier for Vas, because the company switched from using German to English back in the 1990s.

WEDDINGS/CELEBRATIONS. March 16, 2003.Srishti Gupta, a daughter of Dr. and Mrs. Jagdish K. Gupta of Roslyn, N.Y., is to be married today to Vasant Kalathur Narasimhan, a son of Dr. and Mrs. Kalathur Narasimhan of Moorestown, N.J. Sri Rajagopalan, a Hindu priest, is to perform the ceremony at Antun’s Catering in Hicksville, N.Y.The bride, 26, graduated magna cum laude and received a master’s degree in molecular and cellular biology from Harvard.

She met Mr. Narasimhan at the university, where she and Mr. Narasimhan are completing their medical degrees, along with master’s degrees in public policy.

In June, the bride is to become a consultant in the Florham Park, N.J., office of McKinsey & Company, the management consulting business.

The bridegroom, also 26, is currently a consultant, based in Cambridge, Mass., with the international health-equity program of the Rockefeller Foundation; in August, he is also to become a consultant at McKinsey in Florham Park.The bride received a master’s degree in natural science from Cambridge University in England.

His mother, Gita Narasimhan, a former nuclear engineer for Public Service Electric & Gas, is now a lecturer in physics at Burlington County Community College in Pemberton, N.J. His father is the vice president for research and development at the Hoeganaes Corporation, a supplier and developer of industrial raw materials, in the Cinnaminson, N.J.In the past five years, Ms. Gupta and Mr. Narasimhan have worked on medical and policy issues in Africa, Asia and North and South America, but their romance was born on a humble Massachusetts thoroughfare.

”It is on that route we fell in love,” Mr. Narasimhan said.

At the end of the Tanzania project, Mr. Narasimhan took Miss Gupta on what was to be her first camping experience and first attempt at mountain-climbing – up Mount Kilimanjaro.

The River Reporter

Then at the age of about four months, things started to go terribly wrong for the little girl and her parents Christina Marie Lisacchi and her father Anthony Lisacchi, a local plumber by trade.

At first, her folks were told not to worry, things would be OK. But Christina, a certified nursing assistant knew something was wrong, terribly wrong.

The family lived in Roscoe at the time, and when Gabbie was two years and three months old, she awoke from a nap and couldn’t breathe; all the monitors recording her heartbeats registered zero, and the little girl began turning blue.

After rushing her to the Children’s Hospital at Westchester Medical Center, Christina and Anthony were told Gabbie had SMA, a deadly medical condition.

The problem is that the old 1991 Ford E150 gave up the ghost in their driveway after its last outing; they had to jump-start it in front of a local pharmacy while on a mission to get Gabbie her COVID-19 booster shot.

“We’ve invested almost $11,000 in it, but it has electrical problems, the ramp gets stuck,” said Christina, adding that on what proved to be its final journey, the old rusted-out vehicle “Kept shaking and stalling out… we literally almost didn’t make it home from two miles away.” The motor may be dead. Faced with the stark reality that Gabbie desperately needs a new ride, her parents finally located a 2014 Ford E350 handicapped van at a dealership near the city, and put down a deposit of $6,000-“Everything we had saved up”-until they could come up with the rest of the money, without going broke and still have enough cash to buy Gabbie her expensive supplemental foods.

These are Christina Lisacchi’s hopes for Gabriella Rose on the eve of her 13th birthday, and as she embarks on her teenage journeys.

A Breakthrough Treatment Is Helping This Young Artist Stay Focused On Her Craft

Now a breakthrough medication she takes at home has slowed the progression of the rare disease.

HONOLULU – Janelle Fiesta was just a year old and the youngest of three kids when doctors diagnosed her with a severe, progressive neuromuscular disease called spinal muscular atrophy or SMA. The condition affects 1 in 10,000 infants.

It confined her to a wheelchair, so she turned to drawing and at 26 is a very talented anime artist.

Fiesta is also the very first SMA patient in Hawaii to take the first medication for the illness that can be administered at home.

“I’m very grateful for the medication that I’m able to take. Evrysdi gives me the comfort knowing that my SMA won’t progress any further,” she said.

“Very uncomfortable. Very anxiety inducing,” she said.

Fiesta insists her disease doesn’t define her or hold her back.

Spinal Muscular Atrophy Treatment Market Size Of Top Players 2022 With Business Development Plans, Growth Insights, Size And Share Forecast 2028

Spinal Muscular Atrophy Treatment market report gives clear insights into upcoming market trends, revenue, growth status, strategies adopted by top industry players.

Spinal Muscular Atrophy Treatment market report also covers extensive analysis on business development plans, import-export scenario, and demand status of global industry.

According to our latest study, the global Spinal Muscular Atrophy Treatment market size is USD million in 2022 from USD million in 2021, with a change between 2021 and 2022.

What are the key aspects due to which the global Spinal Muscular Atrophy Treatment market is developing? What are the present scenario of Spinal Muscular Atrophy Treatment market in important countries? What will be the opportunity of Spinal Muscular Atrophy Treatment Market? What are the key regions targeted in the forecast year? What are the key attributes, market trends, and recent developments of market? What are the threats and future strategies of Spinal Muscular Atrophy Treatment market?

Spinal Muscular Atrophy Treatment Market Analysis by Regions: Regional analysis is another highly comprehensive part of the research and analysis study of the global Spinal Muscular Atrophy Treatment market presented in the report.

Major Spinal Muscular Atrophy Treatment market players that are involved in the market such as manufacturers, raw material suppliers, equipment suppliers, end users, traders, distributors and etc.

The growth factors of the Spinal Muscular Atrophy Treatment market are discussed in detail where in the different end users of the market are explained in detail.

National Institute Of Neurological Disorders And Stroke

Less common forms of SMA are caused by mutations in other genes including the VAPB gene located on chromosome 20, the DYNC1H1 gene on chromosome 14, the BICD2 gene on chromosome 9, and the UBA1 gene on the X chromosome.

Except in the rare cases caused by mutations in the UBA1 gene, SMA is inherited in an autosomal recessive manner, meaning that the affected individual has two mutated genes, often inheriting one from each parent.

If the SMN1 gene is not found to be abnormal or the individual’s history and examination are not typical of SMA, other diagnostic tests may include electromyography, nerve conduction velocity studies, muscle biopsy, and other blood tests.

In May 2019, the FDA approved onasemnogene abeparovec-xioi gene therapy for children less than 2 years old who have infantile-onset SMA. A safe virus delivers a fully functional human SMN gene to the targeted motor neurons, which in turn improves muscle movement and function, and also improves survival.

Prognosis varies depending on the type of SMA. Some forms of SMA are fatal without treatment.

The National Institute of Neurological Disorders and Stroke, a component of the National Institutes of Health, conducts basic, translational, and clinical research on SMA in laboratories at the NIH and also supports research through grants to major medical institutions across the country.

Animal models of SMA represent critical tools in discovering and developing new therapies for SMA. Scientists have developed zebrafish, mouse, and pig models, including models of less severe SMA types 2 and 3, which may greatly aid the identification of new therapeutic targets and candidate therapies.

Genetic And Rare Diseases Information Center

2012; rarediseases.org/rare-diseases/spinal-muscular-atrophy/.

Diagnosis and management of spinal muscular atrophy: Part 1: Recommendations for diagnosis, rehabilitation, orthopedic and nutritional care.

Diagnosis and management of spinal muscular atrophy: Part 2: Pulmonary and acute care; medications, supplements and immunizations; other organ systems; and ethics.

Kariyawasam D, Carey KA, Jones KJ, Farrar MA. New and developing therapies in spinal muscular atrophy.

Spinal Muscular Atrophy: MedlinePlus Genetics

Other forms of spinal muscular atrophy and related motor neuron diseases, such as spinal muscular atrophy with progressive myoclonic epilepsy, spinal muscular atrophy with lower extremity predominance, X-linked infantile spinal muscular atrophy, and spinal muscular atrophy with respiratory distress type 1 are caused by mutations in other genes.

Most children with spinal muscular atrophy type I do not survive past early childhood due to respiratory failure.

Spinal muscular atrophy type II is characterized by muscle weakness that develops in children between ages 6 and 12 months.

Individuals with spinal muscular atrophy type II cannot stand or walk unaided.

Spinal muscular atrophy type III typically causes muscle weakness after early childhood.

People with spinal muscular atrophy type III typically have a normal life expectancy.

People with spinal muscular atrophy type IV have a normal life expectancy.

Spinal Muscular Atrophy

With proper respiratory support, those with milder SMA type 1 phenotypes, which account for around 10% of SMA 1 cases, are known to survive into adolescence and adulthood even without pharmacological treatment, although they always require round-the-clock care.

Affected siblings usually have a very similar form of SMA. However, occurrences of different SMA types among siblings do exist – while rare, these cases might be due to additional de novo deletions of the SMN gene, not involving the NAIP gene, or the differences in SMN2 copy numbers.

Skeletal problems associated with weak muscles in SMA include tight joints with limited range of movement, hip dislocations, spinal deformity, osteopenia, an increase risk of fractures and pain.

Palliative care in SMA has been standardised in the Consensus Statement for Standard of Care in Spinal Muscular Atrophy which has been recommended for standard adoption worldwide.

Oral salbutamol, a popular asthma medicine, showed therapeutic potential in SMA both in vitro and in three small-scale clinical trials involving patients with SMA types 2 and 3, besides offering respiratory benefits.

Riluzole, a drug that offers limited clinical benefit in amyotrophic lateral sclerosis, was proposed to be similarly tested in SMA; however, a 2008-2010 trial in SMA types 2 and 3 was stopped early due to the lack of satisfactory results.

Whilst stem cells never form a part of any recognised therapy for SMA, a number of private companies, usually located in countries with lax regulatory oversight, take advantage of media hype and market stem cell injections as a “Cure” for a vast range of disorders, including SMA. The medical consensus is that such procedures offer no clinical benefit whilst carrying significant risk, therefore people with SMA are advised against them.

Supplier Of Computer Products From Taiwan

ASUSTOR Inc. was established via direct investment from ASUSTeK Computer Inc. The ASUSTOR brand name was created as a portmanteau of “ASUS” and “Storage”.

ASUSTOR is a leading innovator and provider of private cloud storage and video surveillance solutions, also specializing in the development and integration of related firmware, hardware and applications.

What Is Organizational Culture?

In this article, we explore what organizational culture is, how companies create it, different types of culture and subcultures.

What is organizational culture? Organizational culture is the collection of beliefs, values and methods of interaction that create the environment of an organization.

Why is organizational culture important? The culture in an organization governs many things, from how it makes decisions to how employees interact.

Clan culture If you compare the culture in your workplace to a family, your workplace may possess a clan culture.

How do companies create organizational culture? Company leaders can determine the organizational culture by establishing a company mission statement that applies to all levels of a company’s operations.

Tips for identifying company culture It’s important to determine if a company’s culture is a good fit for you when looking for a new job.

This second set of values is distinct from the larger organizational culture but does not conflict with the wider workplace culture.

8.3 Understanding Organizational Culture – Principles Of Management

The term organizational culture was made popular in the 1980s when Peters and Waterman’s best-selling book In Search of Excellence made the argument that company success could be attributed to an organizational culture that was decisive, customer-oriented, empowering, and people-oriented.

In contrast to a topic such as leadership, which has a history spanning several centuries, organizational culture is a young but fast-growing area within management.

The culture of the organization is closely linked to organizational design.

If a company in the same industry has a culture characterized by stability, a high respect for tradition, and a strong preference for upholding rules and procedures, the company may suffer because of its culture.

In other words, just as having the “Right” culture may be a competitive advantage for an organization, having the “Wrong” culture may lead to performance difficulties, may be responsible for organizational failure, and may act as a barrier preventing the company from changing and taking risks.

In addition to having implications for organizational performance, organizational culture is an effective control mechanism dictating employee behavior.

Key Takeaway Organizational culture is a system of shared assumptions, values, and beliefs that helps individuals understand which behaviors are and are not appropriate within an organization.

What Is Organizational Culture? And Why Should We Care?

While there is universal agreement that it exists, and that it plays a crucial role in shaping behavior in organizations, there is little consensus on what organizational culture actually is, never mind how it influences behavior and whether it is something leaders can change.

If we can define what organizational culture is, it gives us a handle on how to diagnose problems and even to design and develop better cultures.

Sense-making has been defined as “a collaborative process of creating shared awareness and understanding out of different individuals’ perspectives and varied interests.” Note that this moves the definition of culture beyond patterns of behavior into the realm of jointly-held beliefs and interpretations about “What is.” It says that a crucial purpose of culture is to help orient its members to “Reality” in ways that provide a basis for alignment of purpose and shared action.

“Organizational culture the main culture of the society we live in, albeit with greater emphasis on particular parts of it.” – Elizabeth Skringar.

Organizational culture is shaped by and overlaps with other cultures – especially the broader culture of the societies in which it operates.

Trying to assess organizational culture is complicated by the reality that you are trying to hit a moving target.

These perspectives provide the kind of holistic, nuanced view of organizational culture that is needed by leaders in order to truly understand their organizations – and to have any hope of changing them for the better.

Organizational Culture: Definition, Types, Examples

Organizational culture is the set of underlying beliefs, values, principles, and ways of interacting within an organization.

Organizational culture defines what every employee’s behavior should be and how they should interact with the rest of the organization.

Many companies spend a lot of time defining what they want their culture to be so that eventually they don’t even need to call it culture, as it would be part of everyone’s habits.

There are four well known types of organizational culture: Clan, Adhocracy, Hierarchy, and Market.

An example of Hierarchy organizational culture is the military.

General Electric is an example of Market organizational culture.

Business leaders are responsible for designing and communicating the organizational culture they want for their company.

How To Build A Strong Organizational Culture

As a thought leader when it comes to culture and the impact it has on business, I quite frequently get approached by business leaders who want to build a strong organizational culture.

Understanding how to do this starts by understanding what organizational culture is.

For business leaders who want to build a strong organizational culture, the important thing to realize is that culture is a tool – to ensure that your organization functions in the best possible way and to ensure that your organization is recognizable, irrespective of the country of operation and the function in which people operate.

What does this mean in practice? A strong organizational culture can be used to ensure speed and efficiency between colleagues, their work and the outside world.

Let’s say you want to promote the practice of “Taking initiative.” How can you make sure that everyone on the team knows about it? One way is to ritualize the behavior with a public celebration of taking initiative, e.g., an annual “Best initiative” day or “Make a mistake” day.

If you do not measure – such as “Does the person display a sense of decency in day-to-day behavior?” – how can you determine whether or not someone is respectful? If you do not keep tabs on what defines “Efficiency,” how can you determine whether or not an initiative is done in an efficient way?

Building a strong organizational culture is a long journey, one that requires exceptional focus and consistency between the various layers.

Organizational Culture

Corporate culture was already used by managers, sociologists, and organizational theorists by the beginning of the 80s. The related idea of organizational climate emerged in the 1960s and 70s, and the terms are now somewhat overlapping, as climate is one aspect of culture that focuses primarily on the behaviors encouraged by the organization.

Flamholtz and Randle state that: “A strong culture is one that people clearly understand and can articulate. A weak culture is one that employees have difficulty defining, understanding, or explaining.” Strong culture is said to exist where staff respond to stimulus because of their alignment to organizational values.

Organizational culture is taught to the person as culture is taught by his/her parents thus changing and modeling his/her personal culture.

While there is no single “Type” of organizational culture and organizational cultures vary widely from one organization to the next, commonalities do exist and some researchers have developed models to describe different indicators of organizational cultures.

The model is also suited to measure how organizational culture affects organizational performance, as it measures most efficient persons suited to an organization and as such organizations can be termed as having good organizational culture.

Cameron and Quinn designated six characteristics of organizational culture that can be assessed with the Organizational Culture Assessment Instrument.

By assessing the current organizational culture as well as the preferred situation, the gap and direction to change can be made visible as a first step to changing organizational culture.

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As sure as the season brings sunshine, we’re sharing the abundance of Spring.

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Start your day refreshed with a specialty juice from the First Watch juice bar.

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Hungry for seasonal menu updates? Who is First Watch.

First Things First Every season brings change to First Watch, but our commitment to quality and sourcing exceptional ingredients never skips a beet.

We are First Watch – an award-winning daytime restaurant concept serving made-to-order breakfast, brunch and lunch using fresh ingredients.

Since our founding in 1983, we have built our brand on our commitment to operational excellence, our “You First” culture and our culinary mission centered around a fresh, innovative menu that is continuously evolving.

These foundational brand pillars have established First Watch as the largest and fastest growing concept in daytime dining.

We care about our customers, and we care about you! That’s where our YOU FIRST culture begins – each day, we put our employees first and strive to make them happy.

They are empowered with an independence to make decisions that will help provide an exceptional breakfast, brunch, or lunch experience for their customers.

We like to say, we love our employees more than bacon.

We credit our YOU FIRST philosophy as one of the main reasons we were named the fastest growing full-service restaurant chain in 2020.

History Of Watches

The history of watches began in 16th-century Europe, where watches evolved from portable spring-driven clocks, which first appeared in the 15th century.

During the 1980s quartz watches took over the market from mechanical watches, a process referred to as the “Quartz crisis”.

Although mechanical watches still sell at the high end of the watch market, the vast majority of watches as of 2020 have quartz movements.

One account of the origin of the word “Watch” suggests that it came from the Old English word woecce which meant “Watchman”, because town watchmen[when?] used watches to keep track of their shifts.

The pin pallet escapement, an inexpensive version of the lever escapement invented in 1876 by Georges Frederic Roskopf was used in cheap mass-produced watches, which allowed ordinary workers to own a watch for the first time; other cheap watches used a simplified version of the duplex escapement, developed by Daniel Buck in the 1870s.

These kept time with a balance wheel powered by a solenoid, or in a few advanced watches that foreshadowed the quartz watch, by a steel tuning fork vibrating at 360 Hz, powered by a solenoid driven by a transistor oscillator circuit.

Top watches at CES 2017 were the Garmin Fenix 5 and the Casio WSD F20. Apple Watch Series 3 had built-in LTE allowing phone calls and messaging and data without a nearby phone connection.

First Watch Locations Near Me In United States + Reviews & Menu

Want to see all the First Watch United States locations? You’ve come to the right place! Below is a complete list of every First Watch United States location we know of.

If we’ve missed one, be sure to let us know by submitting your review of it on our site.

First Watch specializes in delicious creations freshly-prepared to order.

First Watch begins each morning at the crack of dawn, slicing fresh fruits and vegetables, baking muffins and making French toast batter from scratch.

Their fresh, award-winning Breakfast, Brunch and Lunch dishes are made using only the best ingredients without the use of heat lamps or deep fryers.

The best part is their creative menu features traditional favorites like omelets, pancakes, salads and sandwiches, as well as signature items like the Chickichanga and classic BLTE sandwich.

Their “2 for You” lunch offers half portions of their most popular soups, salads and sandwiches and you can get in and out fast.

Their menu’s “Healthier Side” features a variety of delicious Breakfast, Brunch and Lunch options for the more health-conscious, including egg white omelets, fresh fruit crepes and their signature Power Wrap.

First Watch

Because at First Watch, we begin each morning at the crack of dawn, slicing and juicing fresh fruits and vegetables, baking muffins and whipping up ou.

I’m on a low sodium diet but got to have it! I added a green salad. Love those mixed greens anyway!

Debbie Frieze Burkett That’s a shrimply wonderful idea! Glad you enjoyed it!

How To Choose The Best Company

An individual who purchases an insurance is known as an insured or a policyholder, while the company that offers an insurance is known as an insurance company, or insurer, or underwriter.

Functions of an insurance company/insurance The main function of an insurance company is to provide insurance to cater for unforeseen circumstances which occur beyond the control of a client.

There are various types of insurance companies, but for this article, we will be considering the Allianz worldwide care, the electric insurance, liberty mutual insurance company, rate kick insurance company and esurance insurance company.

Its company offers insurance services which cover life, health and disability insurance.

Electric insurance company offers insurance services for your home, automobile, and umbrella coverages.

Liberty mutual insurance company is an insurance company which offers coverage for individuals, families, and businesses.

Esurance insurance company offers a range of insurance plans to protect clients from an unforeseen event(s).

Protecting What Matters Most

No one can predict the future, but we can certainly prepare for it.

Today’s families are concerned about the bigger picture: healthcare costs, retirement readiness, and protecting their family’s quality of life.

That’s why we’re committed to helping provide holistic solutions designed to help people achieve a lifetime of financial security.

Life insurance from Transamerica helps protect people’s financial future with solutions through every stage of life.

Explore our range of cost effective options below, and rest easy.

Your Dependent’s insurance will terminate the end of the month following the date below which occurs first: the date you cease to be an insured person, unless insurance is continued temporarily as outlined in the section on “Continuance Due to Sick Leave or Leave of Absence” that follows; the date your Dependent ceases to meet the definition of “Dependent” or “Insured person”.

After we acknowledge your disability, We will: continue your Term Life Insurance; waive Premiums for your Term Life Insurance; and require periodic evidence of your continuing disability.

The amount of Life Insurance will depend on whether your coverage amount is based on a multiple of your salary or a flat dollar amount.

Termination of Dependent insurance continued under this provision is concurrent with the termination of a Retired Employee’s Insurance.

GROUP TERM LIFE BENEFITS If an insured person dies while insured under the Group policy, we will pay the beneficiary the amount of Group term life insurance then in effect.

Conversion Privilege You or your Dependents may apply, without evidence, for an individual policy of life insurance to replace all or part of term life insurance that ceases because; your employment has terminated; eligibility for term life insurance has ended; of your death.

If the Group policy terminates or is amended to terminate insurance, the amount convertible will be the amount terminated less the amount of any life insurance for which the insured person becomes eligible under any Group policy within 31 days after termination.

Life Insurance

Skip to content Loading…. Start your Life Insurance quote.

Life insurance provides financial protection for your family in the event of your passing.

Anytime is a good time, but these life events are especially important.

You’ll receive a guaranteed death benefit for the term you choose, and your payments are guaranteed to remain level for the length of the term.

Gives you level premiums, strong guarantees, and valuable protection.

It can also build cash value, which you can access through loans.

Each type of life insurance is designed to meet different needs.

The examiners utilized the information obtained during the examination to assess the Company’s overall potential risks both currently and on an on-going basis, allowing the examiners to focus on the Company’s greatest areas of risk, and to provide assurance on the Company’s financial statements as of the examination date.

NAIC Annual Statement Errors, Omissions, and Misciassifications The examination team found instances in which the Company’s filing of the 2011 NAIC Annual Statement did not conform to the NAIC Annual Statement Instructions and the AP&P. While the Company needs to correct these errors, the following items were not material to the financial statements and no adjustments were necessary.

COMPANY PROFILE Company History The Company was originally incorporated as a Washington stock insurance company on February 21, 1910 as New World Life Insurance Company.

4 Farmers New World Life Insurance Company Farmers New World Life Insurance Company is a stock life insurance company domiciled in the state of Washington and is subject to regulation by the Ole.

The cost to the Company for the 401(k) Savings Plan is included in the overhead and administrative charges paid by the Company to FGI. The Company transitioned from a defined benefit pension plan sponsored by FGI to a Cash Balance Program effective January 1, 2009.

SUBSEQUENT EVENTS On January 1, 2012, the Company entered into a reinsurance agreement with ZIC, a Swiss domiciled insurance company that solely owns FGI. On April 11, 2012, the Company declared an extraordinary dividend in the amount of $105 million, which was paid in cash to FGI on May 16, 2012.

Special Consent The Company holds a special consent, issued by the state of Washington, with an effective date of January 1, 2011, and subsequently renewed effective January 1, 2012, which allows the Company to own and purchase mutual funds if certain statutory requirements have been met.

Life Insurance Corporation

Life Insurance Corporation of India is an Indian statutory insurance and investment corporation headquartered in the city of Mumbai, India.

The Life insurance Corporation of India was established on 1 September 1956, when the Parliament of India passed the Life Insurance of India Act that nationalized the insurance industry in India.

Over 245 insurance companies and provident societies were merged to create the state-owned Life Insurance Corporation of India.

The Oriental Life Insurance Company, the first company in India offering life insurance coverage, was established in Kolkata in 1818.

The Parliament of India passed the Life Insurance of India Act on 19 June 1956 creating the Life Insurance Corporation of India, which started operating in September of that year.

The nationalization of the life insurance business in India was a result of the Industrial Policy Resolution of 1956, which had created a policy framework for extending state control over at least 17 sectors of the economy, including life insurance.

From its creation, the Life Insurance Corporation of India, which commanded a monopoly of soliciting and selling life insurance in India, created huge surpluses and by 2006 was contributing around 7% of India’s GDP. The corporation, which started its business with around 300 offices, 5.7 million policies and a corpus of ₹45.

Welcome to the official twitter handle of LIC India.

For details, contact your LIC Agent or nearest branch.

LIC urges everyone to get vaccinated on time and build a healthy, strong Nation.

LIC is proud to celebrate World Social Work Day with millions of selfless souls that dedicate their lives towards the welfare of others.

NationalNoSmokingDay”You are a woman; that is your superpower.” -Unknown LIC wishes all the women a very Happy Woman’s Day! #BreakTheBias #LICThe Nation owes a great debt of gratitude to the scientists who continue to make lives easier and safer.

LIC salutes them for their passion and contribution.

Lata Mangeshkar – 28 September 1929 – 6 February 2022 LIC joins the Nation in mourning the loss of one of the greatest singers of India.

Securities And Exchange Board Of India

The Securities and Exchange Board of India is the most important regulator of securities markets in India.

SEBI is the counterpart of the Securities and Exchange Commission in the U.S. Its stated objective is “To protect the interests of investors in securities and to promote the development of, and to regulate the securities market and for matters connected therewith or incidental thereto.”

The Securities and Exchange Board of India was established in its current incarnation in April 1992, following the passage of the Securities and Exchange Board of India Act by the nation’s parliament.

It supplanted the Controller of Capital Issues, which had regulated the securities markets under the Capital Issues Act of 1947, passed just months before India gained independence from the British.

SEBI is run by a board of directors, including a chair who is elected by the parliament, two officers from the Ministry of Finance, one member from the Reserve Bank of India, and five members who are also elected by the parliament.

The only mechanisms to check its power are a Securities Appellate Tribunal, which consists of a panel of three judges, and the Supreme Court of India.

It also established the Financial Stability Board in 2009, in response to the global financial crisis, giving the board a broader mandate than its predecessor to promote financial stability.

NSE: NSE Meets Top Brokers On Retail Investor Rush And Its Excesses

The discussions mainly centered around the aggressive practices by some brokers to acquire clients and whether there are enough checks in place while onboarding newbie investors in riskier equity derivatives – mainly options, said three people aware of the development.

The meeting sparked speculation that the Securities and Exchange Board of India could have unofficially nudged NSE to start the groundwork for the contentious product suitability framework for individual investors, a proposal that brokers had strongly opposed.

In the meeting, NSE sought brokers’ feedback on the steps that need to be taken to ensure that retail traders have the knowledge and wherewithal to punt in futures and options, said the people cited above.

Soon after the meeting between NSE and the top brokers during the third week of March, the exchange issued a circular, asking brokers to refrain from ‘unauthorised market practices’ while acquiring clients.

NSE warned brokers against the practice of clients sharing their login and password of trading accounts with people who traded in derivatives on their behalf promising assured returns.

Hordes of new retail investors have opened demat accounts with brokers in the past two years.

NSE said in the March 25 circular that some brokers were running ‘incentives/referral schemes’ to acquire clients which were against the spirit of the exchange’s guidelines.

Individuals Can Use UPI For Bids Of Up To ₹5 Lakh In Public Issues, Says SEBI

Capital markets regulator Sebi on Tuesday said individual investors applying in public issues of equity shares and convertibles can use unified payment interface for application amount up to Rs 5 lakh.

They have been asked to provide their UPI ID in the bid-cum-application form submitted with any of these entities – syndicate member, stock broker, depository participant and registrar to an issue and share transfer agent.

The new guidelines will come into force for public issues opening on or after May 1, 2022, Sebi said in a circular.

The decision has been taken after National Payments Corporation of India reviewed the systemic readiness required at various intermediaries to facilitate the processing of applications with increased UPI limit.

As on March 30, 2022, more than 80 per cent of Self Certified Syndicate Banks/Sponsor Banks/UPI Apps have conducted the system changes and have complied with the NPCI provisions.

In December 2021, NPCI enhanced the per transaction limit in UPI from Rs 2 lakh to Rs 5 lakh for UPI-based Application Supported by Blocked Amount in Initial Public Offers.

SEE ALSO:Rajasthan government pays ₹3,000 crore dues to Adani PowerElon Musk joins Twitter’s board after acquiring a 9.2% stake, says “Significant improvements” coming to the platform.

Securities And Exchange Board Of India Versus Rajkumar Nagpal & Ors. 21 Mar 2022

SEBI’s stand completely disregards the rights of the Debenture Holders of RCFL;. The SEBI Circular is inapplicable as the SEBI Circular cannot be given retrospective effect;.

Of the present case and the circumstances such as the Ld. Single Judge calling upon SEBI to provide a clarification, SEBI being impleaded to the Interim Application, SEBI filing a detailed Affidavit and SEBI’s submissions being taken into account, put the present case on a completely different footing than that of IKISAN. 11.

In view of Regulation 15(2)(b) of SEBI. Regulations, 1993, in case of debt securities issued by way of public issue,.

We are guided first by paragraph no.1 of the SEBI Circular which in one sense is its Preamble and provides “This circular prescribes the process to be followed by the Debenture Trustee(s) in case of ‘Default’ by issuers of listed debt securities including seeking consent from the investors for enforcement of security and/or entering into an Inter-Creditor Agreement”.

Mr. Datar has also argued that the DTDs and Resolution Plan within themselves contemplate the requirement of compliance with securities laws which would include compliance with the SEBI Circular as also the clarificatory letter dated 23rd August, 2021.

As stated herein, in view of the fact that the SEBI Circular is not applicable to the facts of the present case, we fail to appreciate how the clauses of the DTDs and Resolution Plan mandating compliance with securities law can further the case of SEBI and.

At the request of the Learned Advocate appearing for SEBI, status-quo as of today is directed to be continued upto 28th March, 2022.

Securities And Exchange Board Of India

The Securities and Exchange Board of India is the regulatory body for securities and commodity market in India under the ownership of Ministry of Finance , Government of India.

Securities and Exchange Board of India was first established in 1988 as a non-statutory body for regulating the securities market.

The Preamble of the Securities and Exchange Board of India describes the basic functions of the Securities and Exchange Board of India as “…to protect the interests of investors in securities and to promote the development of, and to regulate the securities market and for matters connected there with or incidental there to”.

The Chief Justice of India refused the finance ministry’s request to dismiss the PIL and said that the court was well aware of what was going on in SEBI. Hearing a similar petition filed by Bengaluru-based advocate Anil Kumar Agarwal, a two judge Supreme Court bench of Justice Surinder Singh Nijjar and Justice HL Gokhale issued a notice to the Govt of India, SEBI chief UK Sinha and Omita Paul, Secretary to the President of India.

SEBI’s new norms for Securities exchanges mandates that it should have minimum net-worth of 1 billion and an annual trading of 10 billion.

The Indian Securities market regulator SEBI had given the recognized Securities exchanges two years to comply or exit the business.

If the Securities exchange is not able to achieve the prescribed turnover of 10 billion on continuous basis or does not apply for voluntary surrender of recognition and exit before the expiry of two years from the date of this Circular, SEBI shall proceed with compulsory de-recognition and exit of such Securities exchanges, in terms of the conditions as may be specified by SEBI. Securities Exchanges which are already de-recognised as on date, shall make an application for exit within two months from the date of this circular.

Red Herring Prospectus

Red Herring prospectus refers to the preliminary prospectus filled by the company with SEC generally concerning the initial public offering by the company that contains the information of the company’s operation.

Let us check how such information is disclosed in the Red Herring Prospectus of Twitter, Inc. The information in this preliminary prospectus is not complete and may be changed.

The initial prospectus and the subsequent drafts submitted to the SEC for obtaining approval for public release may be included in the broad term, Red Herring.

Broad Contents of Red Herring Prospectus General definitions and abbreviations.

Other appropriate information about the company, which helps investors make informed decisions…If investors notice any divergence, they can report the same to the SEC. Red Herring prospectus is an initial prospectus filed by the company with the Securities and Exchange Commission.

After being authorized by the SEC, a red herring prospectus tends to become the company’s final prospectus.

Dissimilarities between the red herring prospectus and the prospectus shall be called for attention in the prospectus.

Red Herring Definition

A red herring is a preliminary prospectus filed by a company with the Securities and Exchange Commission, usually in connection with the company’s initial public offering.

A red herring prospectus contains most of the information pertaining to the company’s operations and prospects but does not include key details of the security issue, such as its price and the number of shares offered.

A red herring prospectus may refer to the first prospectus filed with the SEC as well as a variety of subsequent drafts created prior to obtaining approval for public release.

To be considered eligible for release, the SEC must thoroughly review a red herring prospectus to ensure the information contained therein does not include any intentional or incidental falsehoods or statements that are in violation of any laws or regulations.

The term “Red herring” is derived from the bold disclaimer in red on the cover page of the preliminary prospectus.

A red herring prospectus can function as a source of information regarding a potential offering that is currently being crafted by a particular company.

The red herring prospectus contains substantial information on the company as well as information regarding the intended use of proceeds from the offering, market potential for its product or service, financial statements, details regarding pertinent management personnel and current major shareholders, pending litigation, and other pertinent details.

Understanding Its Role From Investor’S Standpoint

In layman terms, a red herring prospectus encloses most of the details regarding the company’s business affairs and future prospects but does not enclose critical share information such as its numbers or price.

Red herring prospectus entails the following sections and usually briefs them out in an explanatory manner to better clarify the company’s financial standing.

A red herring prospectus entails detail regarding the company’s standing compared to its rivals.

It is imperative to dig deeper into this section only after understanding the company’s business affairs and its competition.

If you come out with a finding that the company has yet to clear several due legal cases, it may be beneficial to avoid the IPO. As an investor, you must have the potential to pinpoint the real risk that could jeopardize the company’s growth in the future.

Red herring prospectus serves as a legitimate source for determining a company’s prowess in terms of financial stability.

Although it is a lengthy document, it renders a plethora of crucial information regarding the company’s operations and financials to the potential investor.

Prospectus Red Herring

A red herring prospectus is a formal legal document that is required by and filed with the relevant government financial securities regulator, and provides details about an investment offering for sale to qualified institutional investors or to the public at large, known as retail investors.

There are typically two types of prospectus; the preliminary prospectus, often referred to as “Red herring”, “Draft red herring” or “Draft red herring prospectus” and the Final Prospectus, also referred to as Statutory Prospectus aka Offering Circular.

What Prospectus.com Can Do. For startups, or established companies or funds seeking to raise capital via a formal offering, securities regulators worldwide, as well as investors in a a private offering, require the Issuer to submit a professional red herring prospectus.

The Prospectus.com team of consultants and attorneys can assist with the writing and drafting of your company’s red herring prospectus or other offering documents.

A company going through the stages of an initial public offering must create a prospectus red herring.

A prospectus red herring is needed for issuing debt, this way an investor can make an educated decision about investing.

The most important difference between a final prospectus and a preliminary prospectus is that a preliminary prospectus is NOT an official offering to sell securities and the final prospectus is the official offering document and contains the price of the securities being sold.

What Is A Red Herring Prospectus?

Red Herring Prospectus is a prospectus, which does not have details of either price or number of shares being offered, or the amount of issue.

On the other hand, an issuer can state the issue size and the number of shares are determined later.

An RHP for and FPO can be filed with the RoC without the price band and the issuer, in such a case will notify the floor price or a price band by way of an advertisement one day prior to the opening of the issue.

In the case of book-built issues, it is a process of price discovery and the price cannot be determined until the bidding process is completed.

Such details are not shown in the Red Herring prospectus filed with ROC in terms of the provisions of the Companies Act.

Only on completion of the bidding process, the details of the final price are included in the offer document.

The offer document filed thereafter with ROC is called a prospectus.

Red Herring Prospectus

A red herring prospectus, as a first or preliminary prospectus, is a document submitted by a company as part of a public offering of securities.

A red herring prospectus is issued to potential investors, but does not have complete particulars on the price of the securities offered and quantum of securities to be issued.

The front page of the prospectus displays a bold red disclaimer stating that information in the prospectus is not complete and may be changed, and that the securities may not be sold until the registration statement, filed with the market regulator, is effective.

“Red-herring prospectus” means a prospectus that does not have complete particulars on the price of the securities offered and quantum of securities offered.

Since the registration statement is a very lengthy and complex document, the Securities Act of 1933 requires the preparation of a shorter document, known as a prospectus, for investors to read. The Preliminary Prospectus is distributed during the quiet period, before the registration statement has become effective with the Securities and Exchange Commission.

The name “Red Herring” relates to the red lettered disclaimer displayed on the front page of each preliminary prospectus.

The SEC does not approve the securities registered with it, does not pass on the investment merits, nor guarantee the accuracy of the statements within the registration statement or prospectus.

The Business Professor, LLC

A red herring prospectus includes the information related to the company’s operation and financial status.

All the subsequent drafts of the prospectus are also known as the red herring prospectus until it gets approval for public release.

The SEC may also direct the company to include some mandatory information in the prospectus that is missing in the draft.

The disclaimer asserts the information provided in the prospectus may be subject to change and the information is not complete.

The prospectus includes all the pertinent information about a company, such as the market potential of its products and services.

A red herring prospectus must also include information about the management and current major shareholders.

The SEC does not actually approve a prospectus; rather, they seek to ensure all the relevant information are provided in it and the information is true and correct.

Configuration Management Database

The configuration management database is a database that stores information about configurations items for use in change, release, incident, service request, problem, and configuration management processes.

All this information is structured according to the Tivoli Common Data Model, an information model used to define and share data about configuration items and other artifacts across several Tivoli management products.

The CMDB is maintained by the configuration management component of this product but is also used by other components such as change management, service request management, asset management, and more.

It is a virtual database that includes several types of data from several different sources:Maximo database Contains the actual and authorized versions of configuration item data, as well as information used for security, application and workflow design, reports, and other product functions.

Federated databases Any other databases whose contents you federate with another database.

Can contain additional data regarding configuration items from any source.

Including all these types of data in one virtual CMDB enables you to look at and compare different views of the same configuration item.

Guide To Configuration Management Databases

There is no one-size-fits-all answer to which CIs you should manage within your CMDB. Each organization’s use cases and goals should determine the level of breadth and depth that makes sense for their CMDB set-up.

In general, it makes sense to start high-level and get the services right and then only go wider or deeper where needed to meet your organizational goals.

That said, CIs can be broadly grouped as technical or non-technical entities.

Non-technical entities can also be modeled in your CMDB if you need to represent them as either dependent or impacted by other assets in your IT service mapping.

Lastly, cloud services should be taken into consideration in the design of a CMDB model.

Both SaaS offerings and IaaS offerings can be represented as CIs as needed.

Unlike legacy CMDB’s, Insight for Jira Service Management offers a flexible and open data structure so you can manage all your resources.

Configuration Management Database

The Configuration Management Database SystemAlthough the CMDB system is not explicitly responsible for gathering information about application execution, it does provide the context and data repository necessary to manage it.

Appendix B-Configuration Management DatabaseThere are a multitude of views as to what a configuration management database.

Some define the CMDB and the configuration management system by the strict IT Infrastructure Library definitions, while others rely on one of the many descriptions put forth by vendors of CMDB-related products.

“Let’s put all of IT’s data into one database and call it a Configuration Management Database!”.

“Then let’s keep it in several databases and call it a ‘Federated Configuration Management System!”.

The products that need to be controlled should be identified as configuration items and their details should be recorded in a configuration management database.

Consider the complexity of Figure 11.6., which defines a consistent method to integrate the typical enterprise directory, directory-enabled ITSM work processes, an ITSM configuration management database.

What Is A Configuration Management Database

A configuration management database is often referred to as the heart of your IT service management system.

A configuration management database provides a complete view of the IT configuration items, including Asset Management and Incident Management, their attributes, and their relationships.

Identifying the Configuration Items is an integral function for the development of a configuration management processes.

What is a CMDB? CMDB is an acronym for configuration management database.

Why is having a configuration management database important?

The configuration management database, a fundamental component of ITIL framework, is important to an organization because IT infrastructure is increasing in complexity.

Since any organization’s IT infrastructure could have millions of moving parts because of the ever-changing IT landscape including organizational shifts, new CIs, and configuration changes can be challenging, but it is essential to keep on top of any changes to keep the CMDB optimally functioning thus aiding your service desk.

ITIL Templates And Training Courses

ITIL introduced Configuration Management to remove the Configuration Management Database.

Configuration management is employed to guard and preserve OS configuration files.

4.IT cost Reduction: Having effective and proper configuration management reduces multiple costs in areas such as infrastructure, outsourced services, and management software.

Programmers apply configuration management to view new versions and disseminate the software configuration to additional hosts.

In the banking segment, keen observation is maintained on software employed, components, databases, and facilities concerning configuration management such as service support, incident management, and IT risk management.

Configuration Management serves as s sub-system of the top level of project management systems.

If properly monitored and implemented, Configuration Management guides the project management team to change the product characteristics, representing a proper way to record these changes to meet business requirements for final approvals.

What Is A CMDB?

A CMDB user can visualize each individual IT infrastructure component – for example, a storage device or an application running on a server – which prevents administrative and management errors, helps to ensure regulatory and process compliance, and increases security.

Another benefit of a CMDB is the ability to integrate data from another vendor’s software, reconcile that data, identify any inconsistences within the database and then ensure all data is synchronized.

A CMDB system can also integrate other configuration-related processes, such as change management and incident management, to better manage the IT environment.

Challenges of using a CMDB. A CMDB can also present a number of challenges.

Evolution of the CMDB. Essentially, a CMDB is a single source of truth of configuration information for IT assets, so they can be managed in order to deliver services.

Data management tools can also be used to address the issue of data federation by taking all IT data from a variety of sources and automatically storing it in a CMDB. Such tools increase the accuracy of an enterprise’s CMDB data.

Unified endpoint management and software asset management tools also can be used as data sources for a CMDB to provide visibility for devices within their control.

Configuration Management Database

The CMDB is a fundamental component of ITIL framework’s Configuration Management process.

Federation is usually distinguished from ETL solutions in which data is copied into the CMDB. CMDBs can be used for many things, including but not limited to: business intelligence, software and hardware builds, inventory, impact analysis for change management, and incident management.

The CMDB represents the authorized configuration of the significant components of the IT environment.

The CMDB contains and records data that are also called configuration items.

Configuration management addresses how the data is to be kept up to date.

A configuration item type is the data type of the element or configuration item an enterprise wishes to store within the CMDB. At a minimum, all software, hardware, network, and storage CI types are stored and tracked in a CMDB. As enterprises mature, they start to track business CI types in their CMDB, such as people, markets, products, and 3rd party entities such as vendors and partners.

CMDB schematic structures, also known as database schemas, take on multiple forms.

Lee Van Cleef

Kramer originally wanted Van Cleef for the role of the deputy Harvey Pell, but as he wanted Van Cleef to have his “Distinctive nose” fixed, Van Cleef declined the role in favor of the part of the silent gunslinger Jack Colby.

In 1959, Van Cleef appeared as Luke Clagg in the episode “Strange Request” of the NBC Western series Riverboat starring Darren McGavin, as Jumbo Kane in the episode “The Hostage” on the CBS Western series “Wanted Dead or Alive” starring Steve McQueen, and in an episode of Maverick titled “Red Dog” in 1960 starring Roger Moore and John Carradine.

With his roles in Leone’s films, Van Cleef became a major star of Spaghetti Westerns, playing central, and often surprisingly heroic, roles in films such as The Big Gundown, Death Rides a Horse, Day of Anger, and The Grand Duel.

The band Primus has a song about Lee Van Cleef on their album Green Naugahyde.

The Warcraft universe features the villain Edwin Van Cleef, inspired by Lee Van Cleef.

The Black Library magazine Inferno! featured several short stories, within the Necromunda setting, starring a bounty hunter named Nathan Creed, who was written as a homage to Lee Van Cleef; writer Jonathan Green described the character as “Lee Van Cleef, Clint Eastwood, The Man With No Name and John Wayne all rolled into one”, and illustrations in the magazine clearly showed Creed as physically nearly identical to Van Cleef.

Van Cleef is portrayed by the film’s director Peter Richardson, though it rather suggests Van Cleef the personage is unrealistically playing Tony Benn, a British member of Parliament.

Lee Van Cleef At Brian’S Drive-In Theater

Biography Born Clarence Leroy Van Cleef on January 9, 1925, in Somerville, New Jersey, Lee Van Cleef cultivated an interest in acting following a stint in the Navy during World War II. Immediately before shipping out with the U.S. Navy, Van Cleef married his high school sweetheart, Patsy, in 1943, and the couple eventually had three children.

During his years as a contract player at United Artists and Universal, Van Cleef acted in memorable films such as Kansas City Confidential.

With his film career gone and the end of his first marriage, Van Cleef remarried and tried to rebuild his acting career by taking any role he could find, often small roles on television series.

Van Cleef quickly became an international star in spaghetti westerns playing both villains and heroes.

After production wrapped on the film Thieves of Fortune, Lee Van Cleef was felled by a heart attack at age 64 on December 16, 1989.

Lee van cleef dvds available from amazon.com lee van cleef books available from amazon.com filmography FILMThieves of Fortune with Michael Nouri and Liz Torres.

Lee van cleef now showing Watch Lee Van Cleef’s 1972 spaghetti western The Grand Duel..

What Is A Chief Commercial Officer?

One member of the “c-suite,” so named for their “Chief” titles, is the chief commercial officer, or CCO. This executive helps to ensure the company’s sales and marketing efforts align for success.

In this article, we explain what a chief commercial officer is, describe what a chief commercial officer does, provide the average salary for a chief commercial officer and provide the necessary steps to take to become a chief commercial officer.

CCOs usually report directly to the CEO, or chief executive officer.

What does a chief commercial officer do? The CCO’s specific job duties can vary from company to company depending on the organization’s size and make up.

Scope: The scope of your work is a major factor in how much you make as a CCO. For example, some companies employ both a chief commercial officer and a chief business officer, while others combine the responsibilities into a single CCO position.

For aspiring CCOs, a position in sales is a great way to build the necessary skills to later get a job as a chief commercial officer.

Since there is usually only one CCO per company, you may have to look outside your organization for a CCO opportunity.

Job Description, Salary & More –

If you are interested in finding out more about this job, what the salary is like and what the role involves, you’ve come to the right place.

There’s a lean towards having a marketing background with more and more brands merging the Chief Marketing Officer role and even the CEO role with this new CCO role.

What is the Typical Chief Commercial Officer Salary in the UK? The average salary a Chief commercial Officer in the UK can expect is around the £116,835.

Once you have more than 10 years worth of experience, the salary goes up even more.

Another factor to consider when looking at the salary CCO’s can expect is the location that you are planning to work in that kind of role.

While the CCO is responsible for the commercial development and strategy of a company, the COO or Commercial Operating Officer oversees all manner of business operations, such as manufacturing operations, when applicable, operations research and operations management.

As CCO’s become increasingly in demand, you can now find this job role advertised on many national and international jobs boards such as Jooble.

Chief Commercial Officer: Roles, Responsibilities, And Salary

Many businesses have a Chief Commercial Officer, also known as a CCO. Anyone seeking an exciting career in commercial or online digital media must be well advised to research what it means to be a “Chief Commercial Officer” before starting their new endeavor.

Full of potential, a Chief Commercial Officer can significantly impact the company through strategic planning, budget management, policy development, and execution.

They’re in many cases the only full-time commercial “Generalist” within a company, so their responsibilities are more significant than just advertising and marketing alone.

Chief Commercial Officers are usually apprised of the entire company’s financial status, and it is their job to ensure that all departments are profitable.

The objectives of the Chief Commercial Officer are to ensure that the company must continue to provide products and services that people can be satisfied with.

A Chief Commercial Officer can provide a number of benefits to a company.

The educational background of a Chief Commercial Officer varies depending on the company for which they work.

Chief Commercial Officer

The chief commercial officer is an executive-level role, with the holder being responsible for the commercial strategy and the development of an organization.

It typically involves activities relating to marketing, sales, product development and customer service to drive business growth and market share.

As a corporate officer position, the CCO generally reports directly to the chief executive officer and is primarily concerned with ensuring the integrated commercial success of an organization.

The role typically must combine technical knowledge of the relevant field with strong marketing and business development skills.

Essentially, a CCO takes ownership of the customer and the customer interface with the product or service offering, making sure that all functions of the organization are aligned to meet its strategic commercial objectives.

This means that they are closely linked to the organization’s strategic management function, in drafting, implementing and evaluating cross-functional decisions that will enable an organization to achieve its long-term objectives.

What Are The Responsibilities Of A Chief Commercial Officer?

CCO stands for the Chief Commercial Officer, sometimes also referred to as a CBO. The CCO is typically one of the top-level executives responsible for developing, designing, and approving its commercial strategy.

What are the responsibilities as a Chief Commercial Officer? You will found know it after reading this article.

The importance of a CCO. The CCO makes crucial decisions regarding marketing, sales, product development, and customer service to drive business growth and market share.

To perform the CCO’s role, one must have technical knowledge of marketing and commercial fields with refined marketing skills.

The CCO must have a commercial background with profound knowledge of marketing, direct sales, sales and channel management, developing pricing strategies, and key account management.

Among the major roles, the CCO is responsible for customers, interactions with consumers, offering, launching, and introducing products to meet strategic commercial objectives.

While developing and implementing commercial strategies, the CCO must ensure that it aligns with the company’s objectives and fulfil its annual budget goals.

What Does A Chief Commercial Officer Do?

A Chief Commercial Officer is the person in an organization who is tasked with the strategy and direction of a company or group in areas such as product development, customer service, and marketing.

Much like a chief financial officer or a chief operating officer, the role of a CCO is an executive position that reports directly to the chief executive officer.

As the Internet has grown and opened up new avenues for organizational expansion, more companies are finding the need for chief commercial officers with a strong marketing background to be increasingly important.

This means he or she will also typically be held responsible for working closely with the chief financial officer and any advertising agencies, branding consultants, and creative teams that have been tapped for work on a specific campaign.

If operating within a company that produces a product, one of the chief commercial officer’s duties is to be in touch with, and receive reports from, any engineering teams so he can guide the company’s value for the customer.

The chief commercial officer is in charge of how the customer experiences the company’s brand and how the company delivers the best possible experience for the customer.

Most chief commercial officer jobs require that a candidate have executive experience, a solid educational track record in a related field, and a strong background in marketing and customer service.

The Chief Commercial Officer As A Differentiator

Growth, through sales, is consistently one of the top goals of every for-profit business or organization.

The Advent of the CCO. Over the last decade, the introduction of the Chief Commercial Officer for companies both small and large has resulted from the need to help businesses harness the entire commercial power of the organization.

Before the advent of the CCO, sales responsibilities were singularly centered on the Executive Vice President of Sales or “Head of Sales” who reports directly to a key C-level leader in the organization like the CEO or COO. At first glance, the responsibilities of the CCO and sales leader seem similar.

Sales Leader Responsibilities and Capabilities: The Need for a CCO. Let’s compare the responsibilities and breadth of capabilities of the two sales leader roles: the CCO and the Head of Sales.

Sales leadership development and structure to support the sales people and deals.

Although all of these are included in the broader Chief Commercial Officer role, the CCO through his or her cross-functional and departmental influence, has additional responsibilities.

About the Author: Marc Cottle is an experienced sales leader with 15 years of experience; he is a Principal with McMann & Ransford and leads the Commercial Practice at the company.

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Voters who live in Voter’s Choice Act counties have more days and more ways to vote in the June 7, 2022 Primary Election.

All California active registered voters will receive a vote-by-mail ballot for the June 7, 2022, Primary Election.

California residents are encouraged to use the Secretary of State’s online services or contact staff by email or phone for assistance.

California Governor

The California Dream – the idea that every person can achieve a better life, regardless of where they start out – is central to who we are as Californians.

Even in a time of economic growth and record employment, too many Californians are experiencing the squeeze of stagnant wages and the rising price of building-block necessities such as housing, health care, education, and child care.

We can and must reanimate the California Dream, building a California for All..

Flag, Facts, Maps, Capital, Cities, & Destinations

California, constituent state of the United States of America.

No version of the origin of California’s name has been fully accepted, but there is wide support for the contention that it derived from an early 16th-century Spanish novel, Las sergas de Esplandián, that described a paradisiacal island full of gold and precious stones called California.

California is bounded by the U.S. state of Oregon to the north, by the states of Nevada and Arizona to the east, by the Mexican state of Baja California to the south, and by the Pacific Ocean to the west.

The fluid nature of the state’s social, economic, and political life-shaped so largely by the influx of people from other states and countries-has for centuries made California a laboratory for testing new modes of living.

California’s population, concentrated mostly along the coast, is the most urban in the United States, with more than three-fourths of the state’s people living in the Los Angeles, San Francisco, and San Diego metropolitan areas.

Land Relief The heartland of California is the Central Valley, which runs for 450 miles through the centre of the state, forming a trough between the Coast Ranges to the west and the Sierra Nevada to the east.

The California State Water Project, launched in 1960, is the largest water-transfer system ever undertaken.

California

California Gold RushThe California Gold Rush was sparked by the discovery of gold nuggets in the Sacramento Valley in early 1848 and was arguably one of the most significant events to shape American history during the first half of the 19th century.

California MissionsThe California missions began in the late 18th century as an effort to convert Native Americans to Catholicism and expand European territory.

Baja California SurBaja California Sur’s glorious colonial past has made it a center for historical architecture and traditional art forms, and it’s also a great place to surf and fish.

San FranciscoPerched atop hills and filled-in marshland at the entrance to one of the Pacific’s largest natural harbors, San Francisco has had an outsized influence on the history of California and the United States.

At Four Corners, in the southeast, Utah meets Colorado, New Mexico and Arizona at right angles, the only such meeting of states in the country.

MontanaMontana is the fourth largest U.S. state by area, behind Alaska, Texas and California, but with an average of just six people per square mile, it is one of the country’s least densely populated states.

Although the name Montana is derived from the Spanish montaña of the United States, Alaska was admitted to the union as the 49th state in 1959, and lies at the extreme northwest of the North American continent.

California Maps & Facts

Km, the State of California is located in the western region of the United States.

As observed on the map, California presents the most diverse series of landforms in the entire United States.

Rising to an elevation of 14,505ft it is the highest point in California as well as the highest point in the 48 U.S. States.

Km, California is the 3rd largest and the most populous state in the USA. Located in the north-central part of the state in the Sacramento Valley is Sacramento – the capital and the 6th largest city of California.

Situated in Southern California is Los Angeles – the largest and the most populous city in California.

The State of California is located in the western region of the United States.

California is bordered by the state of Oregon in the north, by Nevada and Arizona in the east, and by the Mexican state of Baja California in the south.

California

California borders Oregon to the north, Nevada and Arizona to the east, the Mexican state of Baja California to the south; and has a coastline along the Pacific Ocean to the west.

The California Gold Rush started in 1848 and led to dramatic social and demographic changes, including large-scale immigration into California, a worldwide economic boom, and the California genocide of indigenous people.

The Spaniards gave the name Las Californias to the peninsula of Baja California and to Alta California, the region that became the present-day state of California.

These new arrivals used the Siskiyou Trail, California Trail, Oregon Trail and Old Spanish Trail to cross the rugged mountains and harsh deserts in and surrounding California.

Most of California’s major rivers are dammed as part of two massive water projects: the Central Valley Project, providing water for agriculture in the Central Valley, and the California State Water Project diverting water from northern to southern California.

The state of California and some California cities, including Los Angeles, Oakland and San Francisco, have adopted sanctuary policies.

At the apex is the seven-member Supreme Court of California, while the California Courts of Appeal serve as the primary appellate courts and the California Superior Courts serve as the primary trial courts.

Drive Medical US Site

Over the past decade, we’ve watched Drive grow from an HME provider to THE HME provider.

It all starts with the people, and theirs are simply top-notch.

Drive Medical Full Product LIne ON SALE NOW

Drive Medical is one of the leading and fastest-growing manufacturers when it comes to mobility aids and home health care assistance products.

Few companies can lay claim to manufacturing as diverse an array of health care products while maintaining the level of professional-grade quality on which Drive Medical has built their name.

From premium wheelchairs for enabling better patient mobility, to their line of bath safety products, such as shower chairs and grab bars, to their top tier oxygen products, Drive’s complete line of products is destined to enhance the life of each user.

Drive Medical is committed to satisfaction by continually offering the highest quality and most functional products in a wide range of health care needs while ensuring the best value and price in their field, all at professional-grade durability.

Their reputation has found their products used and distributed in hospitals, nursing homes, home care facilities, and among individuals throughout North America, Europe, Central America, South America, the Middle East, and Asia, backed by healthcare distributors, professionals, retailers, and more.

Health Products For You

Drive Medical products are focused towards innovation, functionality and value.

Drive Medical products find their use in hospitals, nursing homes, homecare facilities and among individuals.

Drive Medical’s wide range of mobility products exceeds the market expectation for quality, reliability and value.

Drive Medical focuses on innovative and cutting edge products that serve as the foundation of any individual’s mobility.

You can choose Drive Medical products by properties, height, width, depth, weight capacity, material, size, color or price range.

Bath safety products from Drive Medical are designed to be used by adults, children, bariatric or those with a disability.

Drive Medical products for bath safety include specially-designed bathroom aids like shower chairs, transfer benches, commode systems, raised toilet seats, grab bars and safety rails, bath lifts, etc.

Drive Medical, Durable Medical Products

The product information contained in this document, including the product images and additional product materials, was collected from various supplier sources.

All product claims and specifications are those of the product suppliers, not McKesson Medical-Surgical or its affiliates and have not been independently verified by McKesson.

McKesson is not responsible for errors or omissions in the product information.

The properties of a product may change or be inaccurate following the posting or printing of the product information in the document, either in the print or online version.

Caution should be exercised when using or purchasing any products from McKesson’s online or print documents by closely examining the product packaging and the labeling prior to use.

Due to product changes, information listed in this document is subject to change without notice.

This information is placed solely for your convenience in ordering and McKesson disclaims all responsibility for its completeness and accuracy, whether or not the inaccuracy or incompleteness is due to fault or error by McKesson.

Breast Cancer Awareness

Proceeds from the purchase of each Breast Cancer Awareness Cane and Rollator will go to the ACS Making Strides campaign, so you’re not only getting a great, high quality mobility products, but contributing to the fight against breast cancer.

The American Cancer Society does not endorse any product or service.

Drive Medical has paid a royalty fee for the use of the American Cancer Society logo.

Investor Relations :: Pressure BioSciences, Inc.

Pressure BioSciences, Inc. is a leader in the development & sale of innovative, enabling, pressure-based platform solutions for the worldwide life sciences industry.

Our products/services are based on three patented, pressure-enhanced platforms: Pressure Cycling Technology, BaroFold Platform, and Ultra Shear Technology.

There are over 120 publications citing the advantages of the PCT platform over competitive methods, many from key opinion leaders.

The PCT Platform uses alternating cycles of hydrostatic pressure between ambient and ultra-high levels to safely and reproducibly control bio-molecular interactions.

The BaroFold Platform has been shown to remove protein aggregates in biotherapeutic drug manufacturing, thereby improving product efficacy and safety for both new-drug entities and biosimilar products.

The BaroFold Platform can help companies create novel protein therapeutics, accelerate therapeutic protein development, manufacture follow-on biologics, and enable life-cycle management of protein therapeutics.

The UST Platform is based on the use of intense shear forces from ultra-high pressure valve discharge.

Pressure BioSciences Inc. Announces Q4 And Fiscal Year 2021 Results, Provides Business Update

Pressure BioSciences, a leader in the development and sale of innovative, broadly enabling, pressure-based solutions for the worldwide life sciences and other industries, today announced financial results for the fourth quarter and fiscal year ended Dec. 31, 2021.

The company also provided a business update and offered guidance on its strategic changes and growth acceleration planned for FY 2022.

“Building on multiple peer-reviewed opinion leader scientific articles and presentations, accelerating instrument installations, and expanding paid research projects, these platforms are expected to generate important sales growth in 2022 and beyond. In addition, we believe the UST platform is opening up a new, game-changing growth trajectory with its promise for revolutionizing massive global markets from pharmaceuticals, nutraceuticals, cosmetics, agrochem, food/beverage processing, and more.”

Fm/QrNiU. About Pressure BioSciences Inc. Pressure BioSciences is a leader in the development and sale of innovative, broadly enabling, pressure-based solutions for the worldwide life sciences and other industries.

The company’s products are based on the unique properties of both constant and alternating hydrostatic pressure.

PCT is a patented enabling technology platform that uses alternating cycles of hydrostatic pressure between ambient and ultra-high levels to control bio-molecular interactions safely and reproducibly.

Major new market opportunities have emerged in the use of its pressure-based technologies in the following areas: recently acquired, patented technology from BaroFold Inc. to allow entry into the bio-pharma contract services sector, and recently-patented, scalable, high-efficiency, pressure-based Ultra Shear Technology platform to create stable nanoemulsions of otherwise immiscible fluids and to prepare higher quality, homogenized, extended shelf-life or room temperature stable low-acid liquid foods that cannot be effectively preserved using existing non-thermal technologies.

Pressure BioSciences Inc.

Pressure BioSciences, Inc. develops, markets and sells proprietary laboratory instrumentation and associated consumables to the life sciences sample preparation market.

PCT uses alternating cycles of hydrostatic pressure between ambient and ultra-high levels to safely and reproducibly control critical biological processes, such as the lysis of cells, the digestion of proteins, and the inactivation of pathogens.

Pressure BioSciences’ product line is led by its newly released, next-generation Barocycler 2320EXTREME instrument.

Leading scientists are intrigued by Pressure BioSciences’ approach, which among other attributes, revolutionizes the process of rupturing cells for further study, yielding superior biomolecules for investigation.

Pressure BioSciences’ PCT technology utilizes customized, controlled hydrostatic pressure to rupture cells in a chamber, enabling exquisitely customized levels of pressure to optimally break open different types of cells at prescribed pressure levels-something never before accomplished in a commercial setting.

To date, Pressure BioSciences has installed nearly 300 PCT Systems in over 165 leading academic, government, biotech and pharma laboratories around the world.

Pressure BioSciences recently received two patents in China for its novel Ultra Shear Technology, a process that has potential in a wide range of industrial applications, including extending the shelf life of some food products and making two insoluble liquids soluble.

Pressure BioSciences, Inc. To Discuss Fourth Quarter And Fiscal Year 2021 Financial Results And Provide Business Update

Conference Call Scheduled for Tuesday, April 5 at 4:30pm ET. SOUTH EASTON, MA / ACCESSWIRE / April 1, 2022 / Pressure BioSciences, Inc. today announced that the Company will host a teleconference to discuss its Fourth Quarter and Fiscal Year 2021 financial results and to provide a business update.

Anyone interested may listen to the teleconference either live or through a replay approximately one day after the teleconference.

The teleconference will include a Company presentation followed by a Question & Answer period.

About Pressure BioSciences, Inc. Pressure BioSciences, Inc. is a leader in the development and sale of innovative, broadly enabling, pressure-based solutions for the worldwide life sciences and other industries.

Our products are based on the unique properties of both constant and alternating hydrostatic pressure.

PCT is a patented enabling technology platform that uses alternating cycles of hydrostatic pressure between ambient and ultra-high levels to control bio-molecular interactions safely and reproducibly.

Major new market opportunities have emerged in the use of our pressure-based technologies in the following areas: the use of our recently acquired, patented technology from BaroFold, Inc. to allow entry into the bio-pharma contract services sector, and the use of our recently-patented, scalable, high-efficiency, pressure-based Ultra Shear Technology platform to create stable nanoemulsions of otherwise immiscible fluids and to prepare higher quality, homogenized, extended shelf-life or room temperature stable low-acid liquid foods that cannot be effectively preserved using existing non-thermal technologies.

Pressure BioSciences Stock Forecast, Price & News

Pressure BioSciences, Inc. develops and sells pressure-based platform solutions in the Americas, Europe, Asia, Africa, and Australia.

Its pressure cycling technology technology uses alternating cycles of hydrostatic pressure between ambient and ultra-high levels to control the actions of molecules in biological samples, including cells and tissues from human, animal, plant, and microbial sources.

The company offers Barocycler instrumentations comprising Barocycler 2320EXT, Barocycler HUB880, Barocycler HUB440, and The Shredder SG3. It also distributes cell disruption equipment, parts, and consumables.

The company offers Barocycler consumable products, such as PCT MicroTubes, PCT MicroCaps, PCT-Micro Pestle, and pressure used to lyse samples for extraction tubes, as well as application specific kits, including consumable products and reagents.

It serves researchers at academic laboratories, government agencies, biotechnology companies, pharmaceutical firms, and other life science institutions.

The company was formerly known as Boston Biomedica, Inc. Pressure BioSciences, Inc. was incorporated in 1978 and is based in South Easton, Massachusetts.

Pressure BioSciences, Inc. Share Price

Pressure BioSciences, Inc. is a leader in the development and sale of innovative, broadly enabling, pressure-based solutions for the worldwide life sciences and other industries.

Our products are based on the unique properties of both constant and alternating hydrostatic pressure.

PCT is a patented enabling technology platform that uses alternating cycles of hydrostatic pressure between ambient and ultra-high levels to control bio-molecular interactions safely and reproducibly.

Our primary focus is the development of PCT-based products for biomarker and target discovery, drug design and development, biotherapeutics characterization and quality control, soil & plant biology, forensics, and counter-bioterror applications.

Major new market opportunities have emerged in the use of our pressure-based technologies in the following areas: the use of our recently acquired, patented technology from BaroFold, Inc. to allow entry into the bio-pharma contract services sector, and the use of our recently-patented, scalable, high-efficiency, pressure-based Ultra Shear Technology platform to create stable nanoemulsions of otherwise immiscible fluids and to prepare higher quality, homogenized, extended shelf-life or room temperature stable low-acid liquid foods that cannot be effectively preserved using existing non-thermal technologies.

Financial Comparison: Pressure BioSciences Vs. Cytek Biosciences

Pressure BioSciences and Cytek Biosciences are both small-cap medical companies, but which is the superior stock? We will compare the two companies based on the strength of their analyst recommendations, valuation, dividends, institutional ownership, profitability, earnings and risk.

0.0% of Pressure BioSciences shares are owned by institutional investors.

This is a breakdown of recent ratings and price targets for Pressure BioSciences and Cytek Biosciences, as reported by MarketBeat.com.

Cytek Biosciences has a consensus price target of $21.00, suggesting a potential upside of 91.08%. Given Cytek Biosciences’ higher probable upside, analysts plainly believe Cytek Biosciences is more favorable than Pressure BioSciences.

This table compares Pressure BioSciences and Cytek Biosciences’ top-line revenue, earnings per share and valuation.

This table compares Pressure BioSciences and Cytek Biosciences’ net margins, return on equity and return on assets.

Cytek Biosciences beats Pressure BioSciences on 7 of the 9 factors compared between the two stocks.

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Breaking The Traditional Sample Preparation Paradigm With PCT

“While scientists have been well aware of the potential of pressure in theory, the risks of working with high pressure in the laboratory coupled with the lack of commercial instruments have for decades been major deterrents to the use of pressure in scientific research,” mentions Schumacher.

Pioneering the game-changing concept of Pressure Cycling Technology, PBIO commercializes the use of pressure in labs for the high-quality preparation of research samples for biological studies.

PCT is a patented, enabling technology that uses alternating cycles of hydrostatic pressure between ambient and ultra-high levels to safely, conveniently, and reproducibly control the actions of molecules in biological samples.

Using PBIO’s powerful PCT platform, a researcher can manage pressure and turn it on and off, akin to controlling light with a switch.

A biological substance’s reaction time to pressure is instantaneous: by applying pressure to a cell, every biomolecule in or on the cell experiences the same pressure at that given moment as opposed to adding chemicals or using temperature, which usually takes a considerable amount of time to disseminate throughout the cell.

As Pressure BioSciences’ PCT solution can minimize damage to the biomolecules in the cell, it also has the potential to increase the number of ‘needles’ in the ‘haystack’- thus increasing the possibility of discovery.

For the future, in addition to its current use in drug discovery, development, and design, Pressure BioSciences’ growth plan involves expanding PCT to areas such as agriculture, forensics and rape kit testing, non-invasive lipidomic screening of newborns, and more.

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From unboxing to kicking back in cool comfort, our customers are loving the Cocoon by Sealy® Chill mattresses.

Targeted Support Where You Need It.Built with science, made for sleep.

Our signature Posturepedic®Plus Collection features our best quality specialty foams, highest level of targeted support, most advanced motion-absorbing coils, and all-over cooling comfort, for the deep, relaxing sleep you need to take on tomorrow.

Whether you prefer springs, memory foam, or a combination of both- Sealy has a mattress to support your needs.

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Pairs the traditional support of innerspring with the conforming comfort of memory foam.

Sealy Corporation

Sealy is an American brand of mattresses marketed and sold by Tempur Sealy International.

It draws its name from the city where the Sealy Corporation originally started, Sealy, Texas, United States.

Merchant banking firm Gibbons Green Van Amerongen took Sealy private in an April 1989 leveraged buyout, a deal which netted Sealy shareholders US$965m.

In 1990, Ohio Mattress assumed the Sealy name that it had acquired when it purchased Sealy Inc. In 1998 Sealy announced that it was moving from Cleveland to the High Point, North Carolina area.

Although Sealy’s website claims that they are the largest manufacturer of mattresses in the world, Tempur-Pedic had greater revenue than Sealy in 2011.

Sealy sells the majority of its mattresses under its three main brands: Sealy Posturepedic, Stearns & Foster, and Bassett.

The 100,000-square-foot factory outside Shanghai is a joint venture of Sealy China, which is owned and operated by Sealy Inc., and licensee Sealy Australia.

Sealy Posturepedic Mattress Review

Sealy Posturepedic mattresses use Posturepedic Technology™ which provides extra back support in the center third of the mattress.

Sealy Posturepedic mattress prices span from the mid to upper-end.

Sealy Posturepedic makes all types of mattresses including innerspring, all-foam, and hybrid mattresses.

Pros and Cons of Posturepedic Mattresses Pros Cons The additional back support makes Sealy Posturepedic beds good for back pain.

We rigorously test each and every Sealy mattress using our pressure mapping system, in addition to other performance tests, and these 5 Sealy mattresses are the best rated.

Sealy Posturepedic mattresses are available in select stores or online, but not directly from Sealy.

If you do find the mattress that meets your individual criteria, then Sealy Posturepedic is a safe, dependable choice, especially for those who want extra back support for their new mattress.

A Proven Real Estate Investment & Operating Platform

Our fully-integrated platform is built on a foundation of proven deal sense, carefully curated market knowledge, and a clearly defined strategy.

Sealy’s extensive history within our current and target markets, coupled with our reputation of surety to close, has provided access to assets to grow our portfolio using our proven portfolio building strategies.

We believe utilizing our regional offices staffed with hands-on market experts is essential to identifying investment opportunities and market inefficiencies more quickly than our competitors.

TEMPUR-SEALY International

Tempur Sealy International, Inc. is the world’s largest bedding provider.

The company develops, manufactures and markets mattresses, adjustable bases, pillows and other sleep and relaxation products.

Combining a proud history and groundbreaking innovation, the company holds some of the most highly recognized brands in the industry: Tempur®, Tempur-Pedic®, Cocoon™ by Sealy, Sealy®, and Stearns & Foster®.

The Heart & Soul Of Sleep

Sealy – it’s where sleep matters, where sleep is not just “Something we all do”, or “Time spent in bed” but more a question of when, where, why and how we can all sleep better…. That’s why, we are the World’s No.1 Sleep Brand.

Our Story Elevate Ultra Bursting with perfected sleep technology, this is what innovation truly feels like.

View Range Enhance Gel-infused comfort for a restful night’s sleep.

View Range Ortho Plus Prefer a firmer sleeping surface? This collection is designed for you.

Mattresses in the Sealy Enhance, Advantage and Ortho Plus ranges are available in the Small Double size.

Not too big and not too small: a double mattress is perfect for individuals who like to maximise the sleeping area, or couples with a smaller bedroom space to work with.

Ideal for couples who like to stretch out, a King size mattress really adds a touch of luxury to your sleep space.

Keep cool with Sealy moisture-wicking fabric and cool-to-the-touch technology.

Sealy AllergenProtect™ helps keep out common allergens and deposits so your mattress stays fresher than fresh.

Live the dream every night with a Sealy Adjustable Base.

Laying your bed in the spring sun can squash odors and give a fresh air scent #SpringCleaningThe clocks are moving forward tonight for #DaylightSavingsTime, but if you don’t want to move at all, we support that too.

Sealy Care Tip #1: Removing plants from the bedroom can prevent pollen, dust, and insects from moving into your mattress.

Ly/280BwcNParenting is a team effort, and we’re proud to support the dream team from morning to night.

We thought you could use a few treats and a new Sealy Hybrid mattress on your #SealyFirstNight.