Government attacked for ignoring expert advice on nutrition in food parcels – The Guardian

The government has been accused of a shocking disregard for the basic nutrition of the most vulnerable members of society during the pandemic by a group of leading food policy academics.

A letter written by Tim Lang, professor of food policy at Londons City University, was sent early in the Covid-19 crisis to George Eustice, secretary of state for the environment, food and rural affairs, and Duncan Selbie, chief executive of Public Health England.

It called for the creation of an expert committee on food and nutrition to oversee the contents of food packages sent to 1.5 million people required to shield during the pandemicand to the 1.3 million children eligible for free school meals. The letter was co-signed by Erik Millstone, emeritus professor of science policy at the University of Sussex, and Terry Marsden of Cardiff University. They proposed a committee that would mirror the work of Sage, the Scientific Advisory Group for Emergencies, which has informed government policy throughout the crisis.

In its response Defra said that PHE is responsible for the health of the public and the effect of nutrition on our immune system. In turn, PHE replied that the matters raised were for ministers. In effect, neither arm of government believes itself responsible for overseeing nutrition.

Lang described the response as shocking. It shows a troubling failure to put nutrition right at the heart of policy. Its stupid and shows a poor understanding of how inequalities get accentuated in a crisis, he said.

Many of those receiving the free food packages, provided by food service companies Brakes and Bidfood, noted that while they contained fresh fruit and vegetables, they were heavy on simple carbohydrates and low in protein. As schools closed and children eligible for free school meals were given food service company parcels, concerns were also raised about their contents.

Peter Overton, a primary school head teacher in Bristol, posted a picture of one to Twitter, describing it as shameful. The bulk of it was crisps, chocolate biscuits, a loaf of cheap bread, and a block of fat marked for cooking only.

Earlier this month Northumbria Universitys Healthy Living Lab reported a massive decrease in fruit and vegetable intake among pupils eligible for free school meals. Just over half of the children studied said they had eaten no fruit or vegetables in a three-day period after the introduction of lockdown.

Funding for free school meals is now through a weekly 15 voucher per child, which can be spent at nominated retailers. Last week a campaign by Manchester United and England footballer Marcus Rashford forced the government to extend the policy over the summer holiday. While this U-turn was welcomed by child poverty campaigners, there is mounting concern about the nutritional value of the food being eaten by the poorest families.

There has been a real danger that without some sort of oversight we lose focus on basic nutrition, said Naomi Duncan, chief executive of Chefs in Schools, a charity working to improve school meals, which is supporting 850 families during the crisis. The voucher scheme is a financial solution, not a nutritional solution. Theres been a 30-year struggle to get better nutrition at the heart of school food provision and there is a risk of that being lost, she said.

In its response to Lang, Defra argued that leading supermarkets are working to ensure people have the food and products they need. Lang describes this as the key to the problem. Its the leave-it-to-Tesco approach, he said. It shows the weakness of Public Health England.

In a statement PHE said that any decisions about establishing an advisory committee on nutrition would be for ministers to take. Defra declined to comment.

Read From panic buying to food banks: how Britain fed itself in the first phase of cornoavirus in todays OFM.

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Government attacked for ignoring expert advice on nutrition in food parcels - The Guardian

Gut reaction: How the gut microbiome may influence the severity of COVID-19 – The Conversation CA

The risk of severe COVID-19 infection is more common in those with high blood pressure, diabetes and obesity, conditions that are all associated with changes to the composition of the gut microbiome the community of bacteria, viruses and fungi that live in the intestines. This raises the question of whether the gut microbiome has a role in dictating COVID-19 severity.

Lets recap what we know about COVID-19. COVID-19 is a new disease caused by a very contagious virus called SARS-CoV-2.

In most infected individuals, the virus does not cause serious illness. However, it causes a very serious respiratory disease and even death in a minority of patients. Through many studies of people with COVID-19 over the past few months, we have learned what characteristics are more likely to be linked to mild versus severe forms of the disease.

Children and young adults are less likely to develop symptomatic COVID-19, although infection readily occurs in young people with equally high viral loads in the airway, suggesting that they can certainly infect others. In contrast, people of older age and those with pre-existing chronic conditions are highly at risk and very likely develop symptomatic, severe disease.

If we consider the gradient of severity of the disease, children are at one end, and the elderly and patients with chronic conditions are at the other end.

The information collected by researchers from many countries all points to similar characteristics and health conditions that are more commonly seen in patients with severe disease. These include older age, high blood pressure, diabetes and obesity.

The strength of these associations is even more prominent among younger individuals, as younger patients with obesity and diabetes are more likely to have serious disease.

In New York City, 5,279 patients tested positive for COVID-19 between March 1 and April 8, 2020. Of these, 22.6 per cent had diabetes and 35.3 per cent were obese.

Obesity was associated with an increased rate of hospital admission and critical illness. Similar findings were provided by investigators in the United Kingdom about the outbreak in Britain, where obese patients were twice as likely to develop severe disease.

Do these findings raise the possibility that the mechanisms underlying high blood pressure, diabetes and obesity may help explain why these conditions lead to severe COVID-19 disease? Before exploring this question, lets zoom in on cellular and molecular mechanisms known to be involved in COVID-19 disease.

When the virus enters the body, it mostly goes to the airways and the gastrointestinal tract. The virus then binds to specific receptors present on the surface of epithelial cells to enter these cells. Viral replication within the cells leads to cell damage and cell death. This results in the release of specific signalling molecules that alert the local immune system.

Armies of immune cells are then dispatched to initiate an antiviral response. Some of these cells are specialized to locate and identify the virus, while others mount a specific immune attack. The immune response results in the release of cytokines, chemokines and antibodies, which in many cases can defeat the virus, and the patient recovers.

Sometimes the immune system is dangerously at high alert and overreacts. In this case, the immune cells mount an especially strong inflammatory response one that goes beyond what is required to kill the virus. This extra-strong attack releases cytokines and chemokines on a massive scale throughout the body, resulting in a cytokine storm, which causes widespread inflammation and tissue damage in patients with severe COVID-19.

One of the reasons for an abnormal, overreactive immune response lies in the gastrointestinal tract. Millions of interactions are constantly occurring between the immune system and trillions of non-dangerous microbes that live within the body. These interactions educate the immune system in how to function and, importantly, in how not to overreact to infectious microbes. Could this help explain why some people are more likely to develop uncontrolled inflammation upon COVID-19 infection?

The gut microbiome is the community of micro-organisms living inside the gastrointestinal tract, mostly in the large bowel. The microbiome contains bacteria, fungi (yeast), viruses and protozoa, all of which contribute to maintaining a balanced ecosystem and human health. These microbes collectively perform many beneficial functions, including educating the immune system.

When studying the microbiome, scientists examine the composition (what is there) and function (what are they doing) of this ecosystem. We have learned that both composition and function of the gut microbiome are important features linked to human health. In certain conditions, the balance of the gut microbiome composition and function is disrupted in a way that leads to disease, a phenomenon called microbiome dysbiosis.

There is accumulating evidence from animal and human studies that gut microbiome dysbiosis has a causal role in metabolism dysregulation manifested as diabetes and obesity the risk factors of severe COVID-19 disease.

The gut microbiome regulates host defences against viral infections including respiratory viruses, such as influenza virus. This occurs through the activation of immune antiviral mechanisms and the prevention of excessive inflammation.

Different species of the gut microbiome have pro- or anti-inflammatory properties and play different roles in regulating the immune system. In the context of COVID-19, a recent preprint study (not yet peer reviewed) showed that specific members of the gut microbiome were associated with severe disease and with immune markers known to be elevated in severe disease. The association of these gut bacteria with the immune markers was even higher than that of the known risk factors of COVID-19 severity: age and obesity.

Further work is needed to confirm that pro-inflammatory microbial species can contribute to the immune responses that make severe COVID-19 more likely, but based on what we know about the microbiome, this is certainly a possibility. This also could mean that beneficial gut microbiome species, the type that promote low inflammation, have the potential to prevent or remediate the immune alterations that lead to severe COVID-19.

The research community is working very hard to develop and test safe and effective vaccines and treatments against COVID-19. Tapping into the potential of the gut microbiome is another avenue that we can pursue to identify potential safe and affordable probiotics for prevention and treatment. This is not unprecedented in the context of viral respiratory diseases: probiotics and prebiotics can affect the immune response to the flu vaccine, and may improve outcomes in flu-like illnesses.

Until effective treatments are available, mind your microbes and maintain a healthy lifestyle.

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Gut reaction: How the gut microbiome may influence the severity of COVID-19 - The Conversation CA

Testosterone Replacement Therapy Market: Global Industry Trends, Share, Size, Growth, Opportunity and Forecast 2020-2026 – Cole of Duty

Testosterone Replacement Therapy Market Research: Global Status & Forecast by Geography, Type & Application (2016-2026) the new research report adds in kandjmarketresearch.com research reports database. This Research Report spread across 47 Pages, with summarizing Top companies and supports with tables and figures.

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Market Analysis by Type:-

Market Analysis by Applications:-

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The data used to compile the Testosterone Replacement Therapy market report has been collected from different primary and secondary sources. This data has to then be analyzed to verify the accuracy while also being error-free. The data is analyzed according to different parameters, one of which is the SWOT analysis. The data is analyzed to identify the strengths and weaknesses of different companies along with the opportunities that can be exploited and the threats that they face from different directions and opponents.

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Key Players:

The global Testosterone Replacement Therapy market report identifies different companies that occupy a large market share in the Testosterone Replacement Therapy market. These companies are then subjected to a comprehensive analysis to identify different parameters that have contributed to the growth of the market. The popular trends that these companies use to increase the market share that they occupy are also identified. The different advancements in manufacturing technology that has enabled them to gain an edge over other competitors are also listed. The data related to each of the companies has been presented from the year 2016 to the year 2026 and is predicted for the forecast period from the year 2016 to the year 2026.

Market Analysis by Regions:

The Final Report Will Include the Impact of COVID 19 Analysis in This Testosterone Replacement Therapy Industry.

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Testosterone Replacement Therapy Market: Global Industry Trends, Share, Size, Growth, Opportunity and Forecast 2020-2026 - Cole of Duty

Global Testosterone Replacement Therapy Market Trends Analysis, Top Manufacturers, Shares, Growth Opportunities, Statistics & Forecast to 2026 -…

Testosterone Replacement Therapy Market Research: Global Status & Forecast by Geography, Type & Application (2016-2026)

In 2019, the global Testosterone Replacement Therapy Market size was US$ xx million and it is expected to reach US$ xx million by the end of 2026, with a CAGR of xx% during 2021-2026.

Testosterone Replacement Therapy Market is segmented by Type, and by Application. Players, stakeholders, and other participants in the global Testosterone Replacement Therapy Market will be able to gain the upper hand as they use the report as a powerful resource. The segmental analysis focuses on revenue and forecast by Type and by Application in terms of revenue and forecast for the period 2015-2026.The Report scope furnishes with vital statistics about the current market status and manufacturers. It analyzes the in-depth business by considering different aspects, direction for companies, and strategy in the industry.

After analyzing the report and all the aspects of the new investment projects, it is assessed the overall research and closure offered. The analysis of each segment in-detailed with various point views; that include the availability of data, facts, and figures, past performance, trends, and way of approaching in the market. The Testosterone Replacement Therapy Market report also covers the in-depth analysis of the market dynamics, price, and forecast parameters which also include the demand, profit margin, supply and cost for the industry.

The report additionally provides a pest analysis of all five along with the SWOT analysis for all companies profiled in the report. The report also consists of various company profiles and their key players; it also includes the competitive scenario, opportunities, and market of geographic regions. The regional outlook on the Testosterone Replacement Therapy Market covers areas such as Europe, Asia, China, India, North America, and the rest of the globe.

In-depth analysis of expansion and growth strategies obtained by Key players and their effect on competition market growth. The research report also provides precise information on your competitors and their planning. All of the above will help you to make a clear plan for top-line growth.

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Top key players @ Endo International, AbbVie, Eli lilly, Pfizer, Actavis (Allergan), Bayer, Novartis, Teva, Mylan, Upsher-Smith, Ferring Pharmaceuticals, Kyowa Kirin, and Acerus Pharmaceuticals

The main goal for the dissemination of this information is to give a descriptive analysis of how the trends could potentially affect the upcoming future of Testosterone Replacement Therapy Market during the forecast period. This markets competitive manufactures and the upcoming manufactures are studied with their detailed research. Revenue, production, price, market share of these players is mentioned with precise information.

Global Testosterone Replacement Therapy Market: Regional Segment Analysis

This report provides pinpoint analysis for changing competitive dynamics. It offers a forward-looking perspective on different factors driving or limiting market growth. It provides a five-year forecast assessed on the basis of how they Testosterone Replacement Therapy Market is predicted to grow. It helps in understanding the key product segments and their future and helps in making informed business decisions by having complete insights of market and by making in-depth analysis of market segments.

Key questions answered in the report include:

What will the market size and the growth rate be in 2026?

What are the key factors driving the Global Testosterone Replacement Therapy Market?

What are the key market trends impacting the growth of the Global Testosterone Replacement Therapy Market?

What are the challenges to market growth?

Who are the key vendors in the Global Testosterone Replacement Therapy Market?

What are the market opportunities and threats faced by the vendors in the Global Testosterone Replacement Therapy Market?

Trending factors influencing the market shares of the Americas, APAC, Europe, and MEA.

The report includes six parts, dealing with:

1.) Basic information;

2.) The Asia Testosterone Replacement Therapy Market;

3.) The North American Testosterone Replacement Therapy Market;

4.) The European Testosterone Replacement Therapy Market;

5.) Market entry and investment feasibility;

6.) The report conclusion.

All the research report is made by using two techniques that are Primary and secondary research. There are various dynamic features of the business, like client need and feedback from the customers. Before (company name) curate any report, it has studied in-depth from all dynamic aspects such as industrial structure, application, classification, and definition.

The report focuses on some very essential points and gives a piece of full information about Revenue, production, price, and market share.

Testosterone Replacement Therapy Market report will enlist all sections and research for each and every point without showing any indeterminate of the company.

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This report provides pin-point analysis for changing competitive dynamics

It provides a forward looking perspective on different factors driving or restraining market growth

It provides a six-year forecast assessed on the basis of how the market is predicted to grow

It helps in understanding the key product segments and their future

It provides pin point analysis of changing competition dynamics and keeps you ahead of competitors

It helps in making informed business decisions by having complete insights of market and by making in-depth analysis of market segments

TABLE OF CONTENT:

1 Report Overview

2 Global Growth Trends

3 Market Share by Key Players

4 Breakdown Data by Type and Application

5 United States

6 Europe

7 China

8 Japan

9 Southeast Asia

10 India

11 Central & South America

12 International Players Profiles

13 Market Forecast 2019-2025

14 Analysts Viewpoints/Conclusions

15 Appendix

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Global Testosterone Replacement Therapy Market Trends Analysis, Top Manufacturers, Shares, Growth Opportunities, Statistics & Forecast to 2026 -...

COVID19: How Testosterone Replacement Therapy Market Players Are Dealing With The Pandemic? – Cole of Duty

The Testosterone Replacement Therapy Market research provides a brief analysis comprising both primary and secondary research. The report provides the perception of all the key factors somehow affecting Testosterone Replacement Therapy Market. It also includes the degree of competition, product development and opportunities in the global Testosterone Replacement Therapy market which makes it more suitable for market analysis. Moreover, the report covers the latest trends, product dynamics, geographical segmentation and regulatory framework regarding Testosterone Replacement Therapy market.

Request a Sample Copy of the Report https://www.regalintelligence.com/request-sample/141932

Testosterone Replacement Therapy Market prominent players:AbbVie, Endo International, Eli lilly, Pfizer, Actavis (Allergan), Bayer, Novartis, Teva, Mylan, Upsher-Smith, Ferring Pharmaceuticals, Kyowa Kirin, Acerus Pharmaceuticals

Global Testosterone Replacement Therapy market report covers all the key players, driving and restraining factors and opportunities in upcoming years. The report provides the historical revenue of the market, latest trends, market size and utilization for the reference regarding the political and technical environment of Testosterone Replacement Therapy market share.

Enquire or share your queries if any before purchasing the report-

Market segmentation

Market segmentation by type: Gels, Injections, Patches, Other

Market segmentation by application: Hospitals, Clinics, Others

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Testosterone Replacement Therapy market segmentation by region:

The report provides a brief analysis considering both quality and quantity data predicted to provide opportunities evolving the market growth in the forecasting period. Majorly focusing on factors that might affect the market growth makes it more informative.

Key points covered in Report: The information covered in this report are Introduction, Key findings, Market overview, PEST/SWOT Analysis. Factors affecting the growth, Market Size and Trends, Market Segmentation with regional analysis is also included. Assessment with industry overview, company profile and conclusion is also mentioned respectively.

Important Points from Table of Contents:

Global Testosterone Replacement Therapy Market Professional Survey Report 20191 Report Overview1.1 Definition and Specification1.2 Manufacturers and Region Overview1.2.1 Manufacturers Overview1.2.2 Regions Overview1.3 Type Overview1.3.1 Gels1.3.2 Injections1.3.3 Patches1.3.4 Other1.4 Application Overview1.4.1 Hospitals1.4.2 Clinics1.4.3 Others1.5 Industrial Chain1.5.1 Testosterone Replacement Therapy Industrial Chain1.5.2 Upstream1.5.3 Downstream2.1 The Overall Market Performance(Volume)2.1.1 Gels2.1.2 Injections2.1.3 Patches2.1.4 Other2.2 The Overall Market Performance(Value)2.2.1 Gels2.2.2 Injections2.2.3 Patches2.2.4 Other3 Global Testosterone Replacement Therapy Market Assessment by Application3.1 Overall Market Performance (Volume)3.2 Hospitals3.3 Clinics3.4 Others4 Competitive Analysis4.1 AbbVie4.1.1 AbbVie Profiles4.1.2 AbbVie Product Information4.1.3 AbbVie Testosterone Replacement Therapy Business Performance4.1.4 SWOT Analysis4.2 Endo International4.2.1 Endo International Profiles4.2.2 Endo International Product Information4.2.3 Endo International Testosterone Replacement Therapy Business Performance4.2.4 SWOT Analysis4.3 Eli lilly4.3.1 Eli lilly Profiles4.3.2 Eli lilly Product Information4.3.3 Eli lilly Testosterone Replacement Therapy Business Performance4.3.4 SWOT Analysis4.4 Pfizer4.4.1 Pfizer Profiles4.4.2 Pfizer Product Information4.4.3 Pfizer Testosterone Replacement Therapy Business Performance4.4.4 SWOT Analysis4.5 Actavis (Allergan)4.5.1 Actavis (Allergan) Profiles4.5.2 Actavis (Allergan) Product Information4.5.3 Actavis (Allergan) Testosterone Replacement Therapy Business Performance4.5.4 SWOT Analysis4.6 Bayer4.6.1 Bayer Profiles4.6.2 Bayer Product Information4.6.3 Bayer Testosterone Replacement Therapy Business Performance4.6.4 SWOT Analysis4.7 Novartis4.7.1 Novartis Profiles4.7.2 Novartis Product Information4.7.3 Novartis Testosterone Replacement Therapy Business Performance4.7.4 SWOT Analysis4.8 Teva4.8.1 Teva Profiles4.8.2 Teva Product Information4.8.3 Teva Testosterone Replacement Therapy Business Performance4.8.4 SWOT Analysis4.9 Mylan4.9.1 Mylan Profiles4.9.2 Mylan Product Information4.9.3 Mylan Testosterone Replacement Therapy Business Performance4.9.4 SWOT Analysis4.10 Upsher-Smith4.10.1 Upsher-Smith Profiles4.10.2 Upsher-Smith Product Information4.10.3 Upsher-Smith Testosterone Replacement Therapy Business Performance4.10.4 SWOT Analysis4.11 Ferring Pharmaceuticals4.12 Kyowa Kirin4.13 Acerus Pharmaceuticals5 Competitive Lanscape5.1 Global Testosterone Replacement Therapy Capacity (K Units) and Market Share of Manufacturers (2014-2020)5.2 Global Testosterone Replacement Therapy Sales (K Units) and Market Share of Manufacturers (2014-2020)5.3 Global Testosterone Replacement Therapy Revenue (M USD) and Market Share of Manufacturers (2014-2020)5.4 Global Testosterone Replacement Therapy Price (USD/Unit) of Manufacturers (2014-2020)5.5 Global Testosterone Replacement Therapy Gross Margin of Manufacturers (2014-2020)5.6 Market Concentration

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COVID19: How Testosterone Replacement Therapy Market Players Are Dealing With The Pandemic? - Cole of Duty

How to launch a drug in a pandemic? Here’s how 4 drugmakers are using digital tools and fast footwork to do just that – FiercePharma

Launching a new drug is an arduous task even in the best of times. Drugmakers build their commercial teams from scratch, spending months of effort and huge sums of money to ensure their med reaches as many physicians, patients and payers as possible.

Add a global pandemic to that challenging situation, and companies are faced with one of two options: Adapt or fail.

In the early months of COVID-19, drugmakers Esperion, Horizon, Eisai and Clarus, among others, faced thatunexpected hurdle to bringing their drugs to market after years of planning and millions of dollars invested.

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For two, Esperion and Horizon, the pandemic was the backdropand often thedriverfor unexpected success for their novel therapies.In the case of Eisai and Clarus, the pandemic hit like a hammer, leaving both drugmakers scrambling for answers to the new challenge.

These talesof hardship, adaptation and sometimessuccess underscore the pharmaceutical industry's needtoquickly pivot to new ways of communicating during extraordinary circumstances. They also may reveal a new path forward for drugmakers in the uncertain future of global pandemics and, potentially, rolling waves of lockdowns.

Here are their stories.

After nabbing back-to-back FDA approvals for their lipid-lowering game-changers Nexletol and Nexlizet in February, Michigan-based drugmaker Esperion planned an aggressivelaunchto takethe fight right to its pricey PCSK9 class rivals.

Esperion's plan was simple: The drugmaker wouldlaunch Nexletol (bempedoic acid)on March 30 to set the stage for combo therapy Nexlizet (bempedoic acid and ezetimibe, also known as Zetia) to hit the market in July. The company would rely on its 300-strong sales team to reach as many physicians as possible and greasethe wheels for the more effective combo's launch.

Then, COVID-19 struck with only weeks to go before Nexletol took the stage. Facing a full-scale commercial pivot to digital, the only option off the table was delaying the drug'sMarch 30 launch date, CEO Tim Mayleben said.

"There was never a question about whether we were going to launch at that time," Mayleben said."The question internally was 'how do we adapt?'"

RELATED:Esperion scores FDA nod for cholesterol-buster Nexletol

Luckily, Esperion had adopteddigital outreach tactics before the pandemic. The companytasked its field managers with migrating the company'spromotional materials online and leaning into virtual meeting platforms like Zoom and Veeva Engage to replace face-to-face interactions with physicians.

That shift didn't happen overnight, Mayleben said. In fact, it took nearlyamonth post-launch to roll out all the digital tools needed to reach out to physicians effectively. That meant painstakingly building an outreach effort:The company went from a few hundred live engagements each week with physicians early on to a few thousand now, Mayleben said.

But one portion of that arduous effort came with an unexpected result. Esperion launched a virtual speaker series in the last week of April that gave doctors an opportunity to hear more about Nexlizet's pending launch. Not expecting a huge turnout, Esperion was shocked to see enormous attendance numbers for those sessionsfive times the number other drugmakers were getting for similar events, Mayleben saidunderscoring an immense interest in Nexlizet's clinical efficacy.

"We have been absolutely stunned at how successful that has been," Mayleben said.

RELATED:Esperion notches 2nd FDA approval with cholesterol-lowering combo Nexlizet

With doctor feedback pouring in from the series, Esperion accelerated its launch plans for Nexlizet, taking the drug to market in early Junea month ahead of schedule. The decision wasn't an easy one, but after Esperion confirmed doctors' interest and the ability of its supply chain to keep pace, the drugmaker ultimately decided Nexlizet was "the right drug at the right time for physicians and patients."

With lockdowns easing across the board, Esperion's sales team is beginning to return to normalor as close to normal as possiblebut the company's pivot to digital outreach likely won't be going anywhere, Mayleben said.

Having a "nimble" corps of territory managers who are well-versedin virtual outreach tools and equipped with digital promotional materials will remain a high priority in a blended commercial future, Mayleben argued.

"This is our make-or-break moment so we have to be inventive, and that inventiveness makes us more patient-focused," Mayleben said.

Horizon Therapeutics, once a company known for the unsavory practiceofbuying older meds and dramatically raising their prices to turn a profit, has trumpeted aplan in recent years to pin its future on a small stable of successful rare disease drugs.

One of the centerpieces of that plan is Tepezza, a bulging eye drug with blockbuster aspirations approved by the FDA in January.

Tepezza launched immediately after that approval, scoringa six-week head start on the pandemic before its commercial team of 100 was sidelined. For CEO Tim Walbert, that meant making an immediate shift to virtual outreach and helping existing patients find access to clinical sites to receive their Tepezza infusions, even as cities and states were locking down.

"Everything you do is fundamentally changed," Walbert said."The question you face is'have you built the right relationships?'If you haven't, having thatdialogue about your drug's benefits [to] patientsyoure going to be chasing without a lot of success."

RELATED:Horizon notches blockbuster FDA approval for rare eye disease med Tepezza

Despite facing a huge hurdle that early into Tepezza's launch, Walbert acknowledged that just six weeks on the market up front helped in getting initial patients on the drug. Unexpected, however, was how popular Tepezza would be so early into its launch.

Once projecting between $30 million and $40 million in Tepezza sales in 2020, Horizon has now upped its forecast to around $200 million in sales in the first year alone. Even that eye-popping increase is only a fraction of what Horizon believes it could have achieved if COVID-19 hadn't happened.

"We were still able to drive an amazing launchwithout COVID-19, we may have been able to do $500 million in first-year sales," Walbert said.

Having digitalpromotional materials ready to go beforethe pandemic gave Horizon reps the ability to quickly pivot to virtual outreach, but existing relationships with doctors and enthusiasm for the drug's results also paved the way for a successful first six months, Walbert said.

Now, with itsreps beginning to venture back out in the field, Horizon is leaning on those same physician relationships to chart the best path forward.

"Were having to redefine and work with each individual physician and ask, 'what is the best way to communicate?' Walbert said. "Were going and having our reps build a plan for each of our physicians to figure out how we can best serve them."

Eisai had its work cut out for it in marketing its recently approvedinsomnia med Dayvigo, a DEA-scheduled drug launching in a market full of generic competitors.

Dayvigo notched its FDA approval in December but was forced to hold back its launch untilDEA scheduling came through inearlyAprilright in the heart of the COVID-19 pandemic. Unlike other drugmakers that stuck to their launch dates, Eisai decided to postpone the rolloutuntil June 1.

That drastic decision effectively sidelined Eisai's 250-strong commercial team and put the drugmaker nearly two months behind schedule on its physician and consumer outreach, and education campaigns. According to Ivan Cheung, CEO and president of Eisai's global neurology business, the decision was all about "sensitivity" tophysicians'role in fighting COVID-19.

"From our commercial launch preparation, weve been ready for a late March launch for a long, long time," Cheung said. "Its nothing to do with readiness;its really about sensitivityduring the COVID-19 pandemic. We have to bea responsible corporate citizen."

RELATED:Eisai preps for launch with insomnia med Dayvigo after buying out Purdue

However, Eisai said it began to hear from physicians who felt the pandemic madeadequate sleep even more important as lockdowns added pressure to patients' daily schedules.

Reason enough, Eisai thought, to move ahead with the Dayvigo launch. Now,it's working with physicians to establish communication moving forwardand doctors were fine with the high-tech approach.

"What we found is that, given the impact on sleep health, theres a lot of enthusiasm," said Tushar Patel, Eisai's executive director and global lead of sleep-wake disorders in the neurology business group. "The majority of physicians weve spoken to are not only interested in learning about the new medicine, but theyre very open to receiving information digitally."

Eisai has also leaned into its digital outreach to consumers for Dayvigo, hoping to establish a place in an insomnia market jam-packed with generic competitors andMerck & Co.'sBelsomra brand, which hit the scene in 2014.

That outreach plan includes Eisai's "Dayvigo Together" online campaign to connect patients with live nurse educators to help them understand their insomnia symptoms and assess whether Dayvigo could be an effective treatment for them.

Being a huge, global drugmaker comes with some obvious benefits during a pandemic, including the sheer resources to weather the storm. But size isn't everything in times of crisis, a lesson that Clarus Therapeutics learned well in the early months of COVID-19.

Clarus, the maker of oral testosterone replacement tabletJatenzo, had a long road to market: The drug'sFDA approval in April 2019 capped off an arduous, years-long clinical development program, CEO Bob Dudley, Ph.D.,said. And then it had to gear up for launch.

With those past challenges in mind, Jatenzo's February rollout plans represented a big milestone not only for Clarus, but also forDudley, who developed AndroGel's topical formula as CEO at Unimedand is now a big believerin Jatenzo's place in the testosterone replacement field.But just as the launchgotunderway, COVID-19 struckhard.

"[Launching a new drug] isa challenging task, and it turned out to be a lot more challenging than I thought," Dudley said.

RELATED:As COVID-19 social media fatigue sets in, pharma begins to restart other health conversations

Clarus' commercial team of 55 was immediately tasked with unlearning their training in face-to-face physician meetings and pivoting to virtual. For any company, that's a tall task, butClarusmade that shift with remarkable speed, Dudley said.

In the space of a single weekend, Clarus' team came up with a game plan to amp up its digital outreach and get back in front of physicianshungry for new options in testosterone replacement therapies.

"We had all of these well-trained, motivated people with a great message to deliver tohealthcareprofessionals," Dudley said. "It necessitated pivoting on a dime and figuringout how we were going to maintain some semblance of a normal launch."

Speaking to doctors virtually wasn't as easy as showing up at their offices,Dudley said, and often requirednot only educating Clarus' team to use virtual meeting technology but also doctors themselves.

"In some cases, they didnt know how to do it," Dudley said of physicians using meeting technology."We found ourselves not only communicating the message of Jatenzo, but we also had to become experts in that side of it as well.

"The flip side of that was physicians, when they embraced the technology, then we found that they were keenly interested in learning about something new."

Now, after the storm of those early months, Clarus is making the shift back to face-to-face conversations, and Dudley said his team has moved with the same sense of purpose and "nimbleness" that allowed it to succeed during the lockdowns.

What will happen in an uncertain future is still unknown, but Dudley said the lessons learned during the lockdown helped his team preparefor a "blended" commercial future.

"In this environment, you have to be nimble," he said."This is why I think weve been able to maintain forward momentum when it could have justcrashed and burned."

Read more from the original source:
How to launch a drug in a pandemic? Here's how 4 drugmakers are using digital tools and fast footwork to do just that - FiercePharma

2020 Growth: Baobab Ingredient Market 2020 Top Manufactures, Growth Opportunities and Investment Feasibility 2025 – 3rd Watch News

Global Baobab Ingredient Market Research Report Cover Covid-19 Impact

The Baobab Ingredient market research report fabricated by Brand Essence Market Research is an in-depth analysis of the latest trends persuading the business outlook. The report also offers a concise summary of statistics, market valuation, and profit forecast, along with elucidating paradigms of the evolving competitive environment and business strategies enforced by the behemoths of this industry.

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Baobab Ingredient Market is valued at USD 3922.02 Million in 2018 and expected to reach USD 5701.50 Million by 2025 with the CAGR of 5.49% over the forecast period.

Increasing consumption of nutritious food due to associated health benefits including improving digestion, boosting immune system, preventing anaemia and asthma are some major impacting factors driving the growth of the global baobab ingredient market.

Baobab Ingredient can support in weight loss, boosting immunity and detoxifying skin from free radicals. The product is used in nutraceuticals due to its vitamin supplementary qualities. It is an organic, natural protein source that provides a high level of functionality and nutritional benefits. Baobab is an ideal organic protein source containing high level of vitamin C which are used to improved vitamin C deficiency. It is widely used in food, beverages, nutraceutical, personal care & cosmetics and others such as baby foods, soups etc. Also it is used to improve lack of deficiencies diseases. Baobab ingredient can be used in form of pulp, powder and oil. It is rich in potassium, phosphorus, carbohydrates, and vitamin C. Baobab ingredient application has high scope in cosmetics & personal care and food & beverage industry. Baobab powder product is often used as an ingredient in breakfast cereals, cereal bars, granola or crunches. Baobab fruit pulp has a high antioxidant capability mainly because of its high natural vitamin C content. These products are natural and have the ability to cure almost all the types of diseases. It is traditionally used in the treatment of fever, cough, diarrhoea, dysentery, haemoptysis, small pox and measles.

Baobab ingredient market report is segmented on the basis of product, form, application and by regional & country level. Based upon product, baobab ingredient market is classified into pulp, powder and oil. Based upon form, baobab ingredient market is classified into organic and conventional. Based upon application, baobab ingredient market is classified into food, beverages, nutraceutical, personal care & cosmetics.

The regions covered in this baobab ingredient market report are North America, Europe, Asia-Pacific and Rest of the World. On the basis of country level, market of baobab ingredient is sub divided into U.S., Mexico, Canada, U.K., France, Germany, Italy, China, Japan, India, South East Asia, GCC, Africa, etc.

Baobab Foods, LLC

Indigo Herbs Limited

Atacora

Rawsome Foods

Mighty Baobab Limited

Halka B Organics

PhytoTrade Africa

Baobab Fruit Company Senegal

TheHealthyTree Company

Woodland Foods

BAyoba (Pvt) Ltd.

NP Nutra

Simpli Ingredients

Organic Africa

BI Nutraceuticals

Organic Herb Trading

Eco Products

BioessenceTrade

Baobab Foods

Afriplex Pty Ltd.

Aduna Limited

Others.

Baobab Ingredient Market Dynamics

Increasing consumption of nutritious food due to associated health benefits including improving digestion, boosting immune system, preventing anaemia and asthma are some major factors driving the growth of the global baobab ingredient market. According to World Health Organisation, Asthma is the most common chronic disease among children worldwide. Around 339 million people are living with asthma. Over 80% of asthma-related deaths occur in low-and lower-middle income countries. Further, Rise in demand for performance nutrition and beverages, increasing demand for organic products and preference of vitamin C rich organic food are expected to enhance growth of market in coming years. According to NCBI, Scurvy is a clinical syndrome that results from vitamin C deficiency. According to The Centers for Disease Control and Prevention, Vitamin C deficiency (ascorbic acid) has been estimated to occur in 14% of males and 10% of females in the United States. Moreover, increasing consumption of anti-aging products across the globe, growing demand for male grooming products and growth in personal care industry with rising development of natural and organic cosmetic products will enhance growth of baobab ingredient market in forecast peried. However, growing global warming and lack of awareness about the baobab ingredients will hamper the development of baobab ingredient market. Growing concerns related to organic baobab nutritional products and government initiatives to promote organic products will create significant opportunities for the growth of baobab ingredient market during forecast period.

Baobab Ingredient Market Regional Analysis

North America is dominating the baobab ingredient market with the highest share in forecast period due to increasing population shifting from meat-based proteins to plant-based proteins due to various health and environmental concerns. Further, consumption of nutritional supplements, beverages products to improve health, raises awareness among the people about organic food to improve health, established healthcare infrastructure and increasing R&D by major players in this region. According to Plant Based Food Association, One-third of Americans are actively reducing their meat and dairy consumption. As per PBFA, consuming plant-based foods is a trend for Millennials and younger generations that indirectly help to creating enormous market potential for plant-based foods. Moreover, consumption of nutraceutical products to improve health, growing application in food industry for its taste and texture are some of the activities expected to accelerate the market growth in forcaste peried. As per U.S. National Library of Medicine, In the US, the term nutraceutical products are regulated as drugs, food ingredients and dietary supplements and nutraceuticals have received high interests due to potential nutritional and safety profile other than therapeutic capability.

Europe is expected to contribute significant share in the global market due to increasing consumers preference for organic products, rising vegan population and increasing demand from food & beverage sector. Further, growth of baobab ingredient market is enhancing due to the increasing consumption of natural and organic food ingredients and presence of premium cosmetic manufacturers including LOral, Sephora and Chanel have positive industry growth in European countries. According to Food and Drink Federation, The food & drink industry is the biggest manufacturing sector in the country as compared to automotive & aerospace combined industry.

Asia Pacific is expected to dominate global baobab ingredient market with, increasing demand for cosmetics and increasing awareness related to personal hygiene & cleanliness is expected to enhance market growth in this region. China and India are projected to experience vigorous growth followed by other South East Asian countries due to high population provides a significant customer base for personal care, cosmetic, and beauty products. For example, China only spends USD 24 per person annual on personal care and cosmetics products, whereas South Korea and Japan spend USD 171 and USD 174 annually.

Key Benefits for Baobab Ingredient Market Reports

Global Market report covers in depth historical and forecast analysis.

Global Market research report provides detail information about Market Introduction, Market Summary, Global market Revenue (Revenue USD), Market Drivers, Market Restraints, Market opportunities, Competitive Analysis, Regional and Country Level.

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Baobab Ingredient Market Segmentation

By Product: Pulp, Powder, Oil

By Form:-Organic, Conventional,

By Application:-Food, Beverages, Nutraceutical, Personal Care & Cosmetics

Regional & Country AnalysisNorth America, U.S., Mexico, Canada , Europe, UK, France, Germany, Italy , Asia Pacific, China, Japan, India, Southeast Asia, South America, Brazil, Argentina, Columbia, The Middle East and Africa, GCC, Africa, Rest of Middle East and Africa

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To gain insightful analyses of the market and a comprehensive understanding of the impact of COVID-19 is likely to have on the Baobab Ingredient Market during the forecast period between 2020 and 2026, and its commercial landscapeTo learn about the market strategies that are being adopted by your competitors and other leading companiesTo understand the future outlook and prospects of the Baobab Ingredient Market post COVID-19To keep you abreast with the strategies used by other players in theTo understand the changes in rules and regulations in various countries during COVID-19 and its possible effects on the market in the future.

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We publish market research reports & business insights produced by highly qualified and experienced industry analysts. Our research reports are available in a wide range of industry verticals including aviation, food & beverage, healthcare, ICT, Construction, Chemicals and lot more. Brand Essence Market Research report will be best fit for senior executives, business development managers, marketing managers, consultants, CEOs, CIOs, COOs, and Directors, governments, agencies, organizations and Ph.D. Students.

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2020 Growth: Baobab Ingredient Market 2020 Top Manufactures, Growth Opportunities and Investment Feasibility 2025 - 3rd Watch News

Finding The Connection – Entrepreneur

Rajiv Bajaj, Chairman & Managing Director, Bajaj Capital who is also the Founder & Director of OmniLife tells Entrepreneur India on what inspires him

Stay informed and join our daily newsletter now!

June15, 20204 min read

Opinions expressed by Entrepreneur contributors are their own.

You're reading Entrepreneur India, an international franchise of Entrepreneur Media.

I am 50 today and have been working in our family business of wealth management designed for middle income Indians, Bajaj Capital, since the age of 20.

All through these years, I have always pondered- what would I do, if I werent born with this silver spoon and had to take my own path, like many other entrepreneurs.I kept toying with semi- baked ideas like being a Creative Head of anadvertising firm, since I have a dire passion for design, creativity and new ideas.

In my mid- thirties, with my mid- life crisis in full bloom, I intensified the search of finding the true me.I joined Entrepreneurs Organization (EO) around that time and formed a forum along with seven other entrepreneurs, working on goals around business, health, family and self-growth.

As I neared the age of 40, I realisedthe need to find mylife purpose or Ikigai, as it is called in Japanesephilosophy. This ancient wisdom is encoded in every Japanese persons brain and they would know their Ikigai very instinctively.

My curiosity towards this philosophy took me to many places. I visited Okinawa Island in Japan, which is called a Blue Zone, or a centre of healthy longevity,as it has the largest population of healthy centenarians. There, I met several elderly Japanese people and understood the prime and foremost reason behind their long and happy lives they all knew their Ikigai, they all knew how to be happy every day in their daily pursuit of choice, as per National Geographic magazine research.

I also met Professor Akhihiro Hasegawa from Toyo Eiwa University, Japan, who indeed is the only man I know to have done a PHD in Ikigai.I learnt from him that ones Ikigai gives a sense of fullness or value of living, countered to a feeling of emptiness despite immeasurable material success.

Ikigai is a deep emotion; anything which doesnt trigger an emotional response in you cant be your Ikigai.

This journey of researching Ikigai also took me closer to my own Ikigai, which was the study of human longevity and particularly, the interplay between health, wealth and longevity.I realised that helping people discover their Ikigai gives me true joy, and this became my own Ikigai.

Further, this helped me sharpen the mission statement of our company Bajaj Capital to financial well-being over a lifetime, as we stay committed tooffering financial well-being solutions to investors.Therefore, finding my own Ikigaitriggered a series of actions and helped us refine and align our Corporate Mission and discover our Company Ikigai.

This journey also led me and my wife, Anu to find our common Ikigai in total wellbeing, or how to live your life well with full vitality. This led to the birthing of our total wellbeing platform, OmniLife,which became an outcome of our common passion for wellness.

I consider it as a blessing, to wake up each morning with full energy and vigour to work towards my mission.Commercial success is hence, nothing more than a sweet fruit of this labour of love; the true joy is in the journey of following your purpose itself.The Ikigai Venn diagram has truly come alive in our lives, where our vision, mission, passion and profession have all blended together into one.

I invest time over the weekends in coaching people and companies, helping them to explore their Ikigai, and I find true joy in doing the same.

(This article was first published in the Marchissue of Entrepreneur Magazine. To subscribe, clickhere)

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Finding The Connection - Entrepreneur

The left only loves science when it suits their cause – The Post Millennial

Where social media was once the space for artists to expose their talents and for political acts to be exposed, today it has become a minefield of wokerati. In the run-up to a global pandemic, we witnessed how social media has pushed for authoritarianism in demanding curbs to freedom of dissent concerning matters of science where gender identity has been medicalized. Then during the pandemic, we saw this same left suddenly shift only to insist that medical science, even in its early days researching COVID-19, be hailed and rigidly supported.

Raise your hand if you got whiplash watching this bait and switch.

Despite the fact that the science on this coronavirus is far from complete, there are certain scientific facts that have informed public policy, much of it based on the successes of social distancing from the 1918 Spanish flu pandemic: namely social distancing. A cursory glance at how Philadelphia and St. Louis approached the Spanish flu demonstrates a vastly different mortality rates between both cities because of how St. Louis employed social distancing measures within two days of its first case. Conversely, Philadelphia took 16 days to implement social distancing measures which had tragic results: Philadelphias mortality rate was more than double that of St. Louis. Lessons were learned a century ago that seem to not have trickled down through the generations.

Still, science has formed a large part of the social and political discourses throughout the twentieth century to the present and science has improved human longevity over the past 100 years with remarkable success. If it wasnt the dangers of nuclear fission, science was debating the pros and cons of protease inhibitors in the followup care to HIV+ patients. Still as Ebola and SARS, far away from the reality of most of our lives struck thousands, anti-science views came into preponderance in western, mostly anglophone countries since the turn of this century as identity politics sought to usurp scientific discourse and empirical evidence with feelings.

So, the one thing that changed in the initial weeks of the COVID-19 pandemic was an absolute silence in mainstream media, a virtual island retreat vacation from the hokum of identity politics that had been covered in hyperbolic numbers by the mainstream media for the past decade. Its almost as if for a brief moment in time earlier this year that most media understood, finally, the difference between pandering to upper-middle class readers with penchants for reading Pink News while trolling those they dislike on Twitter and those individuals who urgently needed healthcare information while caring for their loved ones.

That vacation, Im afraid to break it to you, dear reader, is now over.

As evidenced by hundreds of death threats and other rather rapey harassment sent to JK Rowling the anti-science mob is back.

Ta-dah! Alas the rampant misogyny from the lips of alleged peace-loving leftists.

All this because of Rowlings response to an earlier bout of harassment for her support of womens rights wherein she quite eloquently exposes her reasons for supporting womens rights.

Aside from this we are facing squarely the after party of where a global pandemic meets fairy dust. Heres the spoiler: it doesnt end well.

Daniel Radcliffe quickly spoke out in disagreement with Rowling stating, Transgender women are women, adding Any statement to the contrary erases the identity and dignity of transgender people and goes against all advice given by professional health care associations who have far more expertise on this subject matter than either Jo (Rowling) or I.

This is a completely anti-science statement for Radcliffe to make given that neither healthcare associations nor doctors make the claim that changing ones sex is possible. Yet, Radcliffe self-isolated during the COVID-19 pandemic and read parts of JK Rowlings Harry Potter to fans across the globe. So what is it? Is a global pandemic a feeling or a reality, or was Radcliffe performing lockdown as part of the larger 5G conspiracy that has been floating about the netherworld in recent months? Radcliffe even apologizes for Rowling in one media report. Welcome to the 19th century where women are spoken for!

Other stars jumped in the mobbing such as Eddie Redmayne who wrote, I disagree with Jo's comments. Trans women are women, trans men are men and non-binary identities are valid. Perhaps Mr. Redmayne ought to consider, therefore, the ire set upon him by trans activists when he took the role of a transgender-identified male, Lili Elbe, in The Danish Girl (2016) disappointing another host of fans who believe that to have the role you must be the person (apparently) in real life.

But wait, what is this you say? Eddie Redmayne has been raising money for Partners In Health (PIH), a nonprofit organization fighting COVID-19 in some of the most vulnerable countries around the world. Its quite odd that when it comes to highlighting their own virtues these actors knows quite well where to put their money, and when it comes to trashing a writer who not coincidentally happens to be female, they know precisely how to cash in on the mobbing.

Heres Ruppert Grint stating more anti-science nonsense, the Ave Maria of gender ideology, Trans women are women, and here he is with a face mask. Me thinks that Grint knows his science when it suits his best interests. And here is Emma Watson decrying Rowlings transphobia. Oh but wait, here she is again virtue signalling for the #IStayHomeFor them campaign. Either Grint or Watson are feigning scientific knowledge about COVID-19 or they are feigning that sex can be changed. It really is that simple.

As one commenter wrote beneath Andrew Doyles discussion with Douglas Murray on woke culture, When victim hood is considered currency there's bound to be counterfeits. There is no more perfect example of the counterfeit culture of wokerati science when in the same sentence you can expound upon the magical, almost Hogwarts-worthy fiction of men becoming women while you wear a face mask telling your fans to stay home. Its time we hold up the counterfeits to the light and move forward with discussing in a civil manner the facts that separate science from fiction.

See more here:
The left only loves science when it suits their cause - The Post Millennial

askST@NLB podcast looks at new ways of working – The Straits Times

With most workplaces shut to stem the spread of Covid-19 during the circuit breaker period, the importance of flexible work arrangements and the use of technology to facilitate remote working came under the spotlight like never before.

Now, as Singapore has entered phase two of reopening its economy, working from home continues to remain the default for most employees.

In the third episode of the askST@NLB podcast series, The Straits Times' manpower correspondent Joanna Seow, along with Singapore Human Resources Institute president Low Peck Kem and Singapore National Employers Federation executive director Sim Gim Guan, considered these new ways of working, as well as the sustainability of the current workforce.

"It took us a crisis to get us going in the direction (of greater digitalisation)," said Ms Seow, adding that this could bring about "transformation in essential service sectors like healthcare, cleaning and public transport". Jobs in these sectors will soon become less labour intensive, owing to telemedicine, robots and autonomous vehicles.

Mr Sim said companies should transform the way they do business. "They will need to upskill and reskill their workers, so that they can take on new jobs or new ways of doing their job," he added.

Aside from acquiring skills in information and communication technology, employees should equip themselves with relevant "analytical, conceptual and evaluative skills", along with interpersonal skills that could help improve their employability, said Mr Sim.

By leveraging technology and redesigning work processes, Singapore will be able to focus on productivity and reduce its reliance on both foreign and local manpower. This is pertinent since the citizen working-age population is expected to shrink from around this year.

To address this, Singapore should "tap older workers, as well as those who are economically inactive", explained Mr Sim. This is where flexible work arrangements will prove crucial.

Many older workers tend to favour part-time work. Those who are economically inactive mainly comprise female workers who have exited the workforce for family and caregiving reasons. Hence, having flexi-work arrangements and schemes like the Professional Conversion Programme could ease them back into the workforce.

Ms Low introduced the idea of "productive longevity" - that living longer entails having people "work longer to ensure (their) retirement adequacy".

"When more services can be delivered digitally or virtually, biases like age, looks, nationality and geographical location get diminished, so people in their 60s or 70s who want to remain active and productive can continue to do so," she said.

The fourth episode of the askST@NLB podcast series, slated for July 3, will feature Straits Times senior food correspondent Wong Ah Yoke and hotelier-restaurateur Loh Lik Peng.

It is titled: The new normal in restaurant dining. The episode will examine how the Covid-19 pandemic has transformed the food and beverage landscape in Singapore.

Readers can send in their questions for the speakers by 6pm on June 28 at str.sg/JPXG.

In the meantime, in order to ensure that flexible work arrangements remain sustainable, especially working from home, a relationship of trust has to be established between the supervisor and the employee. Ms Low stressed that supervisors should seek to understand the challenges of older employees "and provide them with the assurance that (they) will walk the journey with them to have them accustomed to the new way of work".

The 25-minute podcast, which is part of a collaboration between ST and the National Library Board, was released yesterday and is available for free on Spotify, Apple Podcasts, Google Podcasts, the ST Facebook page, radio station Money FM 89.3 and at str.sg/JWfR.

The talks were previously held at the Central Public Library in Victoria Street but they have now become a podcast series recorded remotely in the light of safe distancing measures to guard against Covid-19.

Continued here:
askST@NLB podcast looks at new ways of working - The Straits Times

10 Cars That Have Driven More Than A Million Miles | HotCars – HotCars

All kinds of different cars have made it past the million-mile mark. Most of them didn't even require anything more than regular servicing.

Regardless of the brand or model, wear and tear are inevitable consequences of car usage. Additional factors such as climate, road conditions as well as driving style also impact the condition and state of a vehicle.

This is why regular use of a car would also require performing regular maintenance to ensure that the vehicle performs as well as it should and help in preserving or lengthening its serviceable life. Basic maintenance would be regular cleaning or washing, oil change, and tune-ups, that when added together can help keep the car in good condition.

There are many reported examples of how a well-kept car, despite being regularly used have exceeded both the owner's and manufacturer's expectations with regards to its longevity, which in some cases, carsthat have reached astounding one million in mileage.

While pickup trucks are designed as tough, work-capable machines, the Toyota Tundra of Vic Sheppard is an extraordinary example of how tough a pickup can be when his Tundra managed to hit the million-mile mark bymaking at least 125 thousand miles a year. This feat of extreme mileage on a Tundra was later recognized by Toyota and Mr. Sheppard was given a brand-new Tundra for his achievement.

Related:15 Bad Things That Shorten The Lifespan Of Your Car

As a family vehicle, the Chevy Silverado owned by Hugh and Tammy Penington was both regularly used and maintained, however, the couple was still surprised when their truck managedlive beyond their expectations when after six years, it's odometer reading was at 1.22 million and the truck was still going strong and was recognized by Chevrolet for its longevity.

By virtue of its excellent condition despite its age, an old Mercedes-Benz 280 owned by coupleGeorge and Luzstella Kosche was given one of the best recognitionsa car can have by being returned to its birthplace and displayed in a museum after Mercedes-Benz bought the car from the Kosche's and put the 280 as a display car in Stuttgart.

Already a unique car during its time because of it's the backward-installed engine, a Saab 900 owned by Peter Gilbert was an even more one of a kind car when it exceeded theone million mile mark in 2006.

In another great example of human and machine working hard and breaking barriers is of Farrah Haines, a delivery driver from the US who together with her Hyundai Elantra racked up over a million miles while delivering parts cross-country. Hyundai was impressed enough that she later was given a newer model Elantra as a reward.

Related:14 Pickup Trucks That Will Last You A Lifetime

Known for its excellent build quality and pioneering safety features, Volvo has also earned itself a great reputationfor making really durable cars. This reputation was again bolstered whena long time Volvo fan, Mr. Selden Cooper, who at that time had his second Volvo - a 1987 model 240, hit the million-mile marker in 2012.

In a remarkable case of long time car ownership and partnership, a 1964 Porsche 356C given to Mr. Guy Newmark as a graduation present is still in his possession after over half a century. More amazing though is that the car still runs great and now has over a million miles on it, a fact made possible by regular maintenance according to Mr. Newmark.

While it is expected that Taxicabs would rack up huge mileage during their service life, a 1963 Plymouth Fury has all other cabs beat with it's1.62 million mile mileage. Owned and operated by Joseph Vaillancourt, a Montreal-based taxi driver, this classic car sadlywas in an accident in 1999 thatfinally ended the long-lived taxi.

As Mercedes models go, the 240D is a legendary car not for its looks or extreme supercar performance, but rather for its tank-like build quality. Best illustrated by a 240D taxi unit based in Greece, thisamazing car was owned byGregorios Sachinidis, who was given a brand new C Class by Mercedes-Benz themselves in exchange for his 2.95 million mileage taxi.

Among the longest-lived cars, the surprising winner is a rare 1966 Volvo P1800 that holds the unbelievable odometer reading of over 3million miles (A distance comparable to 7 round trips to the Moon) and is stillin good driving condition. Owned byIrv Gordon, his P1800 was awarded the Guinness world record in 2014.

Next:15 Cars With The Highest Mileage Ever Recorded

Next Here's What We Just Learned About The Eurofighter Typhoon

Karlo watched a lot of Mcgyver back in the 90's and grew up trying to be a Mr. fixit/jack of all trades. A fan of cars and bikes, and most anything with an engine, he divides his time between work and family. A leading business development, project manager in the auction and liquidation industry, and consultant for various local and national government offices in the Philippines. When not at work, Karlo spends his time at home, with family, either being the cook or fixit guy in his house.

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10 Cars That Have Driven More Than A Million Miles | HotCars - HotCars

By Transforming a ‘Stroad,’ Denver Can Move Forward on a Safer, More Inclusive Transportation System – Streetsblog Denver

(Safety-focused Lincoln Street redesign: Dedicated bus lane, traffic-calming lane reduction, bollards, and pedestrian improvements create the conditions for a people-focused multimodal thoroughfare.)

Amanda Roberts is a neighborhood advocate working towards a multimodal future for kids growing up in Denver. Follow her on Twitter @AmandaMtn.

Like many rapidly growing cities across the United States, Denver wrestles with its car-prioritized legacy of interstate building and exit expansions through its increasingly traffic-snarled communities. Just off the Lincoln/Broadway exit today, the dangerous, multilane urban arterial roadway we know as Lincoln Street whisks cars as quickly as possible from I-25 into downtown. Not surprisingly, drivers take full advantage. They speedand they crashplacing Lincoln in the High Injury Network.

Fortunately, Denver has adopted a Vision Zero Action Plan and has started to build out multimodal networks to address its growing traffic crash rate, dedicating bus lanes along downtown and adjacent streets such as Broadway. However, there is one last piece of the puzzle in this transit-oriented area that needs a safety-centric touch: that unique, urban, and mostly residential segment from I-25 to Speer, considered Baker on the west side and Washington Park West on the east side.

Today, its a car-centric stroadan unproductive, unsafe hybrid of a street and a road, on the brink of decline in some areas. But, with a few improvements to the Corridor to increase access and safety for those walking, cycling and taking transit, it can be transformed into a community-first place worth arriving at.

A walk down Lincoln today reveals just how much the street prioritizes cars over people. Drivers regularly travel at speeds well above the posted speed limit of 30mphtypically in the range of 40-50mph, and higher at night. Holding a conversation with another person with street noise at 75-80 decibels is a challenge. Vibrations from fast-moving heavy vehicles such as buses can be felt in adjacent structures, particularly where tree lawns were removed and the distance from doorways to speeding vehicles is minimal. While attempting to access grocery stores, shops, bus stops and light rail, or simply taking a stroll down the street, pedestrians are dodging cars, even in crosswalks. Cyclists have taken to riding on the sidewalks to stay safe.

(North-facing Lincoln Street today, just off the I-25 exit ramp. Though this is a transit-rich area, walking is dangerous since buffer zones to protect pedestrians have been removed to ensure interstate traffic is whisked quickly downtown.)

While the problems of Lincolns dangerous design are numerous and complex, the solutions are already laid out in city plans: Blueprint Denver and Denver Moves: Transit. By reclassifying streets, Blueprint Denver communicates a key distinction between Lincoln and its one-way couplet partner, Broadway. While Broadway maintains its commercial thoroughfare status as a Main Street Arterial, Lincoln Street is reclassified as a Residential Arterial. This new classification takes into account the adjacent land use, and implies that Lincolns street design be similar to parallel north-south Residential Arterials in the area, Logan and Downing. Both of these streets are considered thoroughfares like Lincoln, yet they have two general purpose travel lanes instead of three, two-way traffic flow, and traffic calming elements such as medians and buffer zones with tree lawns and/or parking.

Lincoln Street, however, is unique: as part of the Lincoln/Broadway Corridor, it is also considered a High Capacity Transit Corridor by Denver Moves Transit. This means its a candidate for Bus Rapid Transit or rail, each of which require full bus or rail stop amenities. Fortunately, implementing the goals of each of these documents is straightforward and in line with the Citys goals for Complete Streets Design, which are the citys new guiding principles for the citys public right of way, detailing how we allocate space to transportation, utilities and other public infrastructure. Lincoln Streets general travel lanes can be pared down from three to two, to bring it inline with its new street classification. To meet the citys transit goals for the street, another lane can be dedicated for bus service. And the final lanewhich was removed in the past to move cars and currently is a multi-purpose, difficult-to-manage flex lane that splits bus hours with car parkingcan be permanently transformed into a transit-friendly, easy-to-manage buffer zone.

(Red Carpet Lincoln: Dedicated Offset Bus Lane to provide adequate space for shelters, a buffer zone for a variety of parking types, mixed with in-street tree planters, bollards to limit curb-jumping from crashes, and an asphalt overlay to ensure the longevity of the red paint.)

To get larger numbers of people out of their cars and sustain our urban transit system long-term, we need to go a step further by designing it for human beings. Ill leave this with some questions for consideration. Would you rather:

To address transportation pollution impacts and rising traffic deaths head-on, we need to make the entire experience of transit something that large numbers of people can safely and comfortably opt into. That means we need to invest in repairing the urban spaces that have been cut away in the past to move cars, and redesign our public streetscapes for people so they will choose healthier, safer modes.

The time to do this is now by replacing travel lanes with lower cost tactical transit lanes. Only when we take that step forward will we see a safe, sustainable future for moving people in, out, and around Denver.

Streetsblog Denver informs the movement for sustainable transportation and a livable city. Give $5 per month.

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By Transforming a 'Stroad,' Denver Can Move Forward on a Safer, More Inclusive Transportation System - Streetsblog Denver

Nanobiotix Receives Feedback From US FDA to Advance Phase III Head and Neck Cancer Study Design and CMC Development Plan for NDA – Business Wire

PARIS & CAMBRIDGE, Mass.--(BUSINESS WIRE)--Regulatory News:

With our recent Fast Track designation for NBTXR3 in this patient population, acceptance of the design of our pivotal phase III trial and agreement on our CMC plan, Nanobiotix is well positioned to deliver on our promise of serving the unmet needs of head and neck cancer patients. Our head and neck cancer pathway is our top priority and these developments represent critical milestones that will allow us to administer and supply our trial. We look forward to taking the necessary steps to initiate NANORAY-312 and evaluate the potential of NBTXR3 to improve treatment outcomes for patients around the world. Laurent Levy, CEO of Nanobiotix.

NANOBIOTIX (Euronext : NANO ISIN : FR0011341205 the Company) (Paris:NANO), a clinical-stage nanomedicine company pioneering new approaches to the treatment of cancer, today announced that the FDA has provided necessary feedback regarding the design of NANORAY-312, the Companys pivotal phase III global registration trial in head and neck cancer. The FDA also agreed to the NBTXR3 chemistry, manufacturing, and controls (CMC) Development Plan to support the phase III trial and a future New Drug Application (NDA) for the product.

NANORAY-312: A Phase III Study of NBTXR3 Activated by Investigators Choice of Radiotherapy Alone or Radiotherapy in Combination with Cetuximab for Platinum-based Chemotherapy-ineligible Elderly Patients with Locally Advanced Head and Neck Squamous Cell Carcinoma.

NANORAY-312 will be a phase III investigators choice, dual-arm, randomized (1:1) global registration trial including elderly head and neck cancer patients who are ineligible for platinum-based chemotherapy.

Patients in the control arm will receive radiation therapy with or without cetuximab (investigators choice), and patients in the treatment arm will receive NBTXR3 activated by radiation therapy with or without cetuximab (investigators choice).

The trial is expected to recruit approximately 500 patients. A futility analysis is expected 18 months after the first patient in the trial is randomized, and the interim analysis for progression-free survival (PFS) superiority is expected at 24-30 months. The final analysis will report on PFS and overall survival. Quality of Life will also be measured as a key secondary outcome. In the event of favorable data from the interim analysis, the FDA has advised that NBTXR3 could potentially qualify for accelerated approval.

In support of the phase III trial and a future NBTXR3 New Drug Application (NDA), Nanobiotix met with the FDA in a Type B end-of-phase I meeting on October 16, 2019. Following additional correspondence with the FDA, including written responses to the FDAs recommendations, the Company received written FDA guidance on April 3, 2020. The Company expects to commence NANORAY-312 after making protocol refinements and securing the requisite financing to fund the trial.

Agreement to CMC Development Plan

The FDAs written response regarding the CMC Development Plan does not raise any safety concerns for continued clinical development of NBTXR3, and the FDA agreed to the updated CMC Plan for NBTXR3 during an ongoing phase III clinical trial.

***

About NBTXR3NBTXR3 is a first-in-class product designed to destroy tumors through physical cell death when activated by radiotherapy. NBTXR3 has a high degree of biocompatibility, requires one single administration before the first radiotherapy treatment session, and has the ability to fit into current worldwide standards of radiation care. The physical mode of action of NBTXR3 makes it applicable across solid tumors.

NBTXR3 is actively being evaluated in clinical trials worldwide as a potential treatment in various cancer indications. The Company is prioritizing the development of NBTXR3 in the United States and the EU for the treatment of patients with locally advanced head and neck cancers ineligible for chemotherapy.

Nanobiotix is also running an Immuno-Oncology development program, evaluating NBTXR3 activated by radiotherapy as a primer of immune response in combination with checkpoint inhibitors. The Company has launched a phase I clinical trial of NBTXR3 activated by radiotherapy in combination with anti-PD-1 checkpoint inhibitors in patients with locoregional recurrent (LRR) or recurrent and metastatic (R/M) head and neck squamous cell carcinoma (HNSCC) amenable to re-irradiation or with lung or liver metastasis (mets) from any primary cancer eligible for anti-PD-1 therapy.

Other ongoing NBTXR3 trials are treating patients with liver cancers (hepatocellular carcinoma and liver metastasis), locally advanced or unresectable rectal cancer in combination with chemotherapy, head and neck cancer in combination with concurrent chemotherapy, and pancreatic cancer. The Company has a broad, comprehensive clinical research collaboration with The University of Texas MD Anderson Cancer Center (initially expected to support nine new clinical trials in the United States) to evaluate NBTXR3 across several cancer types.

About NANOBIOTIX: http://www.nanobiotix.com Incorporated in 2003, Nanobiotix is a leading, clinical-stage nanomedicine company pioneering new approaches to significantly change patient outcomes by bringing nanophysics to the heart of the cell.

The Nanobiotix philosophy is rooted in designing pioneering, physical-based approaches to bring highly effective and generalized solutions to address unmet medical needs and challenges.

Nanobiotixs first-in-class, proprietary lead technology, NBTXR3, aims to expand radiotherapy benefits for millions of cancer patients. Nanobiotixs Immuno-Oncology program has the potential to bring a new dimension to cancer immunotherapies.

Nanobiotix is listed on the regulated market of Euronext in Paris (Euronext: NANO / ISIN: FR0011341205; Bloomberg: NANO: FP). The Companys headquarters are in Paris, France, with a US affiliate in Cambridge, MA, and European affiliates in France, Spain and Germany.

Disclaimer

This press release contains certain forward-looking statements concerning Nanobiotix and its business, including its prospects and product candidate development. Such forward-looking statements are based on assumptions that Nanobiotix considers to be reasonable. However, there can be no assurance that the estimates contained in such forward-looking statements will be verified, which estimates are subject to numerous risks including the risks set forth in the universal registration document of Nanobiotix registered with the French Financial Markets Authority (Autorit des Marchs Financiers) under number R.20-010 on May 12, 2020 (a copy of which is available on http://www.nanobiotix.com) and to the development of economic conditions, financial markets and the markets in which Nanobiotix operates. The forward-looking statements contained in this press release are also subject to risks not yet known to Nanobiotix or not currently considered material by Nanobiotix. The occurrence of all or part of such risks could cause actual results, financial conditions, performance or achievements of Nanobiotix to be materially different from such forward-looking statements.

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Nanobiotix Receives Feedback From US FDA to Advance Phase III Head and Neck Cancer Study Design and CMC Development Plan for NDA - Business Wire

Disordered proteins follow diverse transition paths as they fold and bind to a partner – Science Magazine

Shedding light on disordered proteins

Disordered proteins often fold as they bind to a partner protein. There could be many different molecular trajectories between the unbound proteins and the bound complex. Most methods to measure transition paths rely on monitoring a single distance, making it difficult to resolve complex pathways. Kim and Chung used fast three-color single-molecule Foster resonance energy transfer (FRET) to simultaneously probe distance changes between the two ends of an unfolded protein and between each end and a probe on the partner protein. They show that binding can be initiated by diverse conformations and that the molecules are held together by non-native interactions as the disordered protein folds. This allows the association to be diffusion limited because most collisions lead to binding.

Science, this issue p. 1253

Transition paths of macromolecular conformational changes such as protein folding are predicted to be heterogeneous. However, experimental characterization of the diversity of transition paths is extremely challenging because it requires measuring more than one distance during individual transitions. In this work, we used fast three-color single-molecule Frster resonance energy transfer spectroscopy to obtain the distribution of binding transition paths of a disordered protein. About half of the transitions follow a path involving strong non-native electrostatic interactions, resulting in a transition time of 300 to 800 microseconds. The remaining half follow more diverse paths characterized by weaker electrostatic interactions and more than 10 times shorter transition path times. The chain flexibility and non-native interactions make diverse binding pathways possible, allowing disordered proteins to bind faster than folded proteins.

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Disordered proteins follow diverse transition paths as they fold and bind to a partner - Science Magazine

Case Medical Awarded Patent for Multi Enzymatic Solution for Cleaning Medical Devices and Food Industry Utensils and Surfaces Exposed to Brain Wasting…

Patent is a significant step toward commercializing cleaning products to effectively inactivate and degrade prions

Case Medical today announced that it was awarded U.S. patent number 10,699,513 B2, by the U.S. Patent and Trademark office for "compositions and methods for handling potential prion contamination." The patent is a significant step for the company toward commercializing cleaning products that will enable prion contaminated devices and surfaces to be processed without resorting to the extraordinary methods required today.

Prions are a type of protein that can cause unfolding in normal prion proteins most commonly found in the brain, but also in the spine, eye, spleen, and lymphoid tissues. Prion diseases are described by the CDC as "a family of rare progressive neurodegenerative disorders that affect both humans and animals. They are distinguished by long incubation periods, characteristic spongiform changes associated with neuronal loss, and a failure to induce inflammatory response." The CDC also indicates that "the abnormal folding of the prion proteins leads to brain damage... Prion diseases are usually rapidly progressive and always fatal."

Prions are transmitted by eating of meat infected with prions, but also in healthcare settings from blood transfusions and from medical devices, especially from surgical instruments, even from apparently cleaned devices, having residual prion contamination.

"The challenge with prions is that they are almost impossible to detect before a fatal occurrence of the disease and they are also extremely hard to remove from contaminated devices and surfaces," said Marcia Frieze, CEO of Case Medical. "The logical solution would be to make prion decontamination a standard part of medical device processing but the current options are extremely time consuming and so harsh that they significantly reduce the useful life of the devices themselves."

Currently, prion contaminated materials are either incinerated or pre-treated with sodium hypochlorite, sterilization, oxidizing agents, peracetic acid, or pre-treatment at temperatures above 100C for extended periods of time. These methods and materials are environmentally unfriendly and excessively corrosive to the materials being cleaned. The cleaning solution patented by Case Medical uses a multi enzymatic formulation to achieve a safer, more thorough result and requires much less time and effort, suggesting a feasible process for healthcare settings and the food processing industry.

In brief, Case Medicals formulation uses specific enzymes combined with a surfactant. The enzymes effectively digest or inactivate prions rendering them ineffective and the surfactant lowers the level of friction to allow easy rinsing. The process is easy, biodegradable, and environmentally preferred.

"While prion diseases are currently rare and a much bigger issue in Europe than in the U.S., the coronavirus pandemic has hopefully taught us the value of being prepared," said Frieze. "We still have many regulatory steps before we can fully commercialize this product and process, but we are continuing to work as fast as we can."

Testing and validation were performed in conjunction with the U.S. Geological Service (USGS) through their National Wildlife Health Center at the Class III prion lab in Madison, Wisc.

About Case Medical

Case Medical is a FDA registered, ISO certified manufacturer of validated, sustainable, and cost effective products for instrument processing. Our reusable sterilization containers and instrument chemistries meet the highest standards for patient safety and environmental preference. Case Medical was an inaugural recipient of the U.S. EPA Safer Choice Partner of the Year award. Visit http://www.casemed.com for more information.

View source version on businesswire.com: https://www.businesswire.com/news/home/20200616005865/en/

Contacts

Lisa Forsell, Director of MarketingPhone: 201-313-1999 x302Email: lforsell@casemed.com Web: http://www.casemed.com

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Case Medical Awarded Patent for Multi Enzymatic Solution for Cleaning Medical Devices and Food Industry Utensils and Surfaces Exposed to Brain Wasting...

Morgan Stanley’s CEO Said He Is ‘Committed’ to Diversity. A Lawsuit Filed by the Firm’s Former Diversity Head Alleges Otherwise. – Institutional…

Earlier this month, Morgan Stanleys chief executive officer James Gorman shared a planon LinkedInto improve diversity at the bank.It included promotions for certain Black employees, the creation of an Institute of Inclusion and a $5 million donation to the NAACP.

On Tuesday, less than two weeks later, the firms former diversity head, Marilyn Booker, filed a lawsuit against Morgan Stanley alleging racial discrimination. The suit was filed on behalf of herself and her former Black female colleagues in the U.S. District Court in the Eastern District of New York.

Booker is suing Morgan Stanley, her former supervisor Barry Krouk, and Gorman for alleged discrimination and retaliation in violation of the Civil Rights Act of 1866, alleged discrimination and retaliation in violation of the New York State Human Rights Law, and alleged violations of both the Equal Pay Act and the New York Equal Pay Law. Booker has also filed an Equal Employment Opportunity Commission complaint, according to her lawsuit.

We strongly reject the allegations made in this claim and intend to vigorously defend ourselves in the appropriate forum, a Morgan Stanley spokesperson said. We are steadfast in our commitment to improve the diversity of our employees and have made steady progress while recognizing that we have further progress to make. We will continue to advance our high priority efforts to achieve a more diverse and inclusive firm.

Booker, who was fired from the firm in December, had worked at Morgan Stanley for 26 years, according to her complaint.

She spent about 16 years as the firms global head of diversity before allegedly being shuffled around through different departments. In 2010, she was moved to the office of development, which was eliminated in 2011. That year, she was selected to lead the firms urban markets group, overseeing minority financial advisors.

Booker alleged in the lawsuit that her salary was essentially held flat in that role as the firm slashed its budget for the program year after year.

According to Bookers complaint, she tried to create a plan to internally address the firms racial biases in 2019. Her plan, called Project Genesis was created with the goal of addressing Morgan Stanleys Black employees constant feelings of isolation and lack of support.

This included addressing their alleged inability to join financial advisory teams and barriers to partnering with white financial advisors on new business opportunities, including unfair commission splits and exclusion from new client meetings. According to the lawsuit, less than one percent of the firms financial advisors are Black.

Krouk, her supervisor, allegedly helped Booker identify analysts and executives who could help Booker on the project last year.

However, Krouk allegedly later told Booker not to tell her colleagues about the project, and allegedly stalled when she asked to present the project to senior management.

A meeting Booker allegedly expected to cover the project was scheduled in December 2019. During it, though, Booker was fired from the firm, the complaint said.

Despite her longevity, loyalty and stellar performance record, Morgan Stanley offered no explanation for her expulsion other than to vaguely say that her position which is one that primarily helps Black people and people of color gain financial literacy and acumen had to be eliminated, the lawsuit said.

[II Deep Dive: The Story Behind Shundrawn Thomass Open Letter to Asset Management]

Gormans plan to improve diversity at the firm, shared on June 4, includes the creation of a similar initiative: the Institute of Inclusion. This group will set up policies and metrics to track diversity and will oversee mentoring, development, and promotion of the firms diverse employees. The announcement said that Morgan Stanley will set aside $25 million for the initiative.

This is the second discrimination lawsuit filed against Morgan Stanley this year. In late April, a female former financial advisor at the firm alleged in a lawsuit that she missed out on pay and was harassed by co-workers because she is a woman,Institutional Investorssister publicationRIA Intelreported at the time.

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Morgan Stanley's CEO Said He Is 'Committed' to Diversity. A Lawsuit Filed by the Firm's Former Diversity Head Alleges Otherwise. - Institutional...

dr-simon-whitesman-on-why-mindfulness-is-medicine – Longevity LIVE

Gisele Wertheim Aymes speaks to Dr. Simon Whitesman (MBChB) about why mindfulness is medicine. Dr. Whitesman is a practitioner of medical psychotherapy at Christiaan Barnard Memorial Hospital in Cape Town and chairman of the Institute of Mindfulness.

A: I always wanted to be a doctor. However, when I became one, the experience was nothing that I had imagined. There was a strong missing element. Then a colleague suggested I start meditating. I had heard of TM, so I went and did TM training. This helped me become very disciplined, and it made a relatively quick and deep impact on my physical well-being. I had suffered from tension headaches and now found relief. And it was this that started my scientific interest in meditation.

When I read Quantum Healing by Deepak Chopra, I experienced an epiphany. It was like walking into a room I had been in and recognizing everything.

It resonated with me. This idea that raising consciousness is the basis for all healing like a key fitting into a lock.

And from there I began an exploration of this insight. I have walked many paths as a psychotherapist. From mind-body connection and Buddhist contemplative therapies to more contemporary approaches to mindfulness. This is where I have really found more meaning now in a more contemporary approach to mindfulness.

A: I discovered it was about my own healing a parallel process while wanting to find expression as a clinician and a doctor. And then recognizing a symmetry on the inside that was compelling for me, in terms of my own path and personal growth.

Then, through Jon Kabat-Zinns work, I was exposed to mindfulness, which is not the same as TM.

Jon Kabat-Zinn is an American professor emeritus of medicine, and creator of the Stress Reduction Clinic and the Center for Mindfulness in Medicine, Health Care and Society at the University of Massachusetts Medical School, in the US. Kabat-Zinn was a student of Zen Buddhist teachers such as Philip Kapleau, Thich Nhat Hanh and Seung Sahn, and a founding member of the Cambridge Zen Center. His practice of yoga and studies with Buddhist teachers led him to integrate their teachings with scientific findings. He teaches mindfulness, which he says can help people cope with stress, anxiety, pain, and illness. The stress-reduction program created by Kabat-Zinn, mindfulness-based stress reduction (MBSR), is offered by medical centers, hospitals, and health-maintenance organizations.

A: The original roots of mindfulness are part of a set of teachings from Buddha 2 500 years ago. Buddha was a human who woke up to who he was and developed a way of teaching others to help them wake up. Central to this path was mindfulness. There were obviously many other aspects, but mindfulness was central.

Kabat-Zinn understood that there are so many people who could benefit from mindfulness, but who were not necessarily interested in Buddhist teachings. He developed mindfulness around keeping the essential qualities of Buddhism, but without the beliefs. You could say it is Buddhism without the belief. Its a contemporary re-contextualization of ancient wisdom and tradition. This meant that if you were a Catholic priest, you could benefit from mindfulness; it didnt conflict with your own set of beliefs. This was a subtle, but very important shift.

A: Mindfulness enables you to be more compassionate, more present, less reactive. Its meditation made more accessible.

Kabat-Zinn first offered it in a contemporary tertiary teaching hospital in Worcester, Massachusetts. He saw it could be a benefit for so many those suffering from chronic pain syndrome, the people who fall through the cracks. He told colleagues to send them to him. Kabat-Zinn taught these patients how to turn inward, to find a new way of being in pain. From there, his work expanded into other chronic disorders.

Medicine doesnt want to go there. I saw that, but for me, there is a desire to bring it back to my life. For me, it is not so much about mindfulness, but more heartfulness.

A: I went to the US and started training in that approach. While I had learned the TM technique, Jon Kabat-Zinn helped to orientate me to what meditation truly is.

What are you going to do when you finish meditation? When you finish meditating, can you make the next moment valuable, engaged, connected, awake, with a quality of curiosity, interested in your own experience? Its valuable to meditate, but the application is deeper than sitting and closing your eyes. Dedicate time to understanding your own mind. Its a willingness to explore and be interested in your own experience.

You dedicate time to silence, to understand your own mind better. Then I also need to get up and go to the world, be present in the world. Its always available to us. Awareness isnt going anywhere. Awareness is now, attending to each and every moment of our lives. Then life becomes meditation.

If you do take time to be with yourself, understand your relationship between body and mind, then life becomes a meditation. Its a radical shift in understanding, broadly and universally applicable. . Mindfulness isnt about thought; its prior to thought. Train yourself to be aware of the thought prior to its occurring.

A: Yes, agreed. We get lost in thinking. We lose a wider presence with our body. Most of us are lost in thinking the revered space between our left and right ear. And we lose our consciousness of Earth and others. You have to start with mindfulness of the body, then mindfulness of thoughts. And it becomes a trainable skill, an actual physiological skill transforming our own awareness. Not randomly, but in service of the greater good, to reduce our own suffering, then the suffering of others. In order to experience a more meaningful existence and live life, we have to train our minds.

When you train for the Two Oceans, you train your body extensively. You cant run a marathon if you havent trained physically. People think the mind is easier. Its not. Youre asking people to open up and be uncomfortable. Gym is not comfortable; gym can be hard. Its the same as training for consciousness. It isnt easy, but it is simple.

Mindfulness is about focusing on the present, not worrying about yesterday or tomorrow.

A cartoon shows two Buddhist monks sitting side by side. Theyre deep in meditation when the younger one opens an eye and gives the older, wiser one a questioning look.

Nothing happens next. This is it, the older one responds.

I treat mindfulness daily in my practice, and I teach an eight-week program on mindfulness. We are training professionals in mindfulness at the Faculty of Medicine at Stellenbosch University. Its much broader than doctors. We train the trainers through the Faculty of Medicine and Health Sciences. This is the only university in South Africa that offers this course. I also contribute towards IMEISA, a non-profit around mindfulness, to create more awareness and debunk myths around mindfulness.

Everyone can benefit from mindfulness. However, the only way you will know the benefit is if you practice. It will be in your own experience. However, for me, I saw my own changes: reduced reactivity and stronger connection with myself and others, as well as everything around me. Its the human condition to be lost in thought. We cant connect if were not present. Something happens when we dont make our mind the enemy. Be more engaged in the moment. Its not an idea; its a truth.

This is how mindfulness can heal trauma. Read more.

Apart from his role as a practitioner of medical psychotherapy at Christiaan Barnard Memorial Hospital in Cape Town, Dr Simon Whitesman is the co-ordinator of the post-graduate certificate training in Mindfulness-Based Interventions at Stellenbosch Universitys Faculty of Medicine and Health Sciences. Hes also director and chairperson of the Institute for Mindfulness South Africa (IMISA), and co-director of the first Mindfulness-Based Stress Reduction (MBSR) program in South Africa. He received certification as a teacher in MBSR from the University of Massachusetts Center for Mindfulness, and in psychoanalytic psychotherapy from the South African Institute for Psychotherapy.

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dr-simon-whitesman-on-why-mindfulness-is-medicine - Longevity LIVE

When It Comes To Device And Website Security, Automation Is More Important Than Ever – Forbes

CEO ofSectigo, driving innovation in digital identity and cybersecurity for today's enterprises, including automation, IoT and DevOps.

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The world faces an unprecedented global health crisis. As governments race to protect the health and well-being of their citizens, businesses must find innovative ways to serve clients and customers. Although countless employees in a wide range of industries have been asked to work remotely to prevent further spread of the new coronavirus, these businesses must continue producing. For many, this represents a unique opportunity to improve and modernize their practices.

Much-needed changes that organizations have been meaning to get to will now become paramount. Manual management of an environment by group participation works when the group is together in a common area, but when the group is dispersed, the tasks become exponentially riskier and more challenging. That means the need for automation is now. Businesses that embrace automation will realize its full benefits, while laggards will suffer from risk and inefficiency in our increasingly complex business world.

Automation has become essential to countless business processes, from manufacturing to fielding customer service calls. But many areas of business are still ripe for automation, particularly in IT. In the new work-from-home reality, IT departments must enable secure remote access for dispersed workforces. Automating important website security processes enables IT personnel to focus on other business-critical tasks while preventing costly lapses in protection. Automation solutions are usable by employees with limited technical skills. Manual processes, in contrast, often are built by experts who provide little by way of documentation or training materials. Should these experts become nonessential, the business would suddenly be at great risk.

Workforce Disruptions Can Generate Security Lapses

Digital certificates are a critical aspect of website and device security, and we have already seen an earlier example of how a workforce disruption can affect them. The U.S. federal government shutdown of 2018-19 furloughed hundreds of thousands of government employees, including IT personnel who were unable to conduct routine operations such as issuing and renewing expiring certificates. As a result, many government services and websites went offline during the 35-day shutdown, including more than130 online services and applications in a single week. Affected websites ranged from the U.S. Court of Appeals to NASAs rocket testing website.

Manual certificate maintenance requires careful management. For instance, browsers will only trust a website certificate for a certain term length (at present two years, but soon dropping to one). That means more certificates will require renewal, or browsers will no longer trust the site. If IT departments are unable to track upcoming certificate expirations for timely renewal, they risk their sites being flagged as untrustworthy and critical systems going offline. In fact, many high-visibility service outages for major digital systems stem from certificate management errors. December 2018sday-long service outagefor 32 million O2 customers is a perfect example.

Todays global workforce disruption dwarfs the 2018 government shutdown in scale and longevity. The biggest shake-up so far stems from shutting down office locations in favor of employees homes, introducing a new set of needs and risks and catching many IT departments off guard. As time goes on, this new norm will take a further toll on businesses as workforces struggle with adversity in many forms:

These factors combine to place extreme risk on any human-intensive process in the enterprise, especially one as intolerant of delay or error as certificate renewal.

Automation can eliminate expiration-based outages, cut mistakes and free up IT professionals time for other projects. It does not require in-depth institutional knowledge, and administrators can easily configure and operate automated systems.

Getting Started With Certificate Automation

Thinking of embarking on a certificate automation project? You may already have started. Microsoft CA is Microsofts built-in certificate management system, and it enables automatic management of certificates within Windows environments. For those using Windows in any capacity, it is a valuable first step into automation. Of course, few organizations operate exclusively in Windows, which means Microsoft CA is best used in conjunction with other services capable of managing certificates for all operating systems and use cases.

When adding a new system, it is wise to conduct an inventory of existing certificates. An automated certificate discovery tool can do this for you. In addition to identifying production certificates before they expire and create a crisis, you also can ensure all certificates are following mandated security practices and meeting appropriate compliance requirements.

Make sure you find a solution that provides interoperability with your critical systems those you use today and those youre likely to expand to in the future. To ensure interoperability, look for these capabilities:

Adjusting To The Present Is Also Planning For The Future

With IT teams still working to adjust to the new normal, they are discovering that now is the perfect time to automate essential business practices. Many organizations expect newly automated processes and more flexible work-from-home policies to remain in placewell after the current crisis, so ensuring that they are prepared to face the IT and security challenges that go along with our new reality anywhere, anytime is of paramount importance.

Forbes Technology Council is an invitation-only community for world-class CIOs, CTOs and technology executives. Do I qualify?

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When It Comes To Device And Website Security, Automation Is More Important Than Ever - Forbes

Why Strange New Worlds is the show Star Trek and the world needs right now – GamesRadar+

Whats in a name? When it comes to Star Trek TV shows, a title says a hell of a lot. The opening credits of The Next Generation were enough to tell us it was Trek for, well, a new generation; Voyager implied a crew on a long journey; Picard instantly made it clear that the mission was a man. Prequel series Enterprise tried to make a statement by removing Star Trek from its name entirely though it did wind up reinstating it for season three when the producers realised their mediocre efforts at subterfuge were fooling nobody.

The recently announced Star Trek: Strange New Worlds has arguably the most evocative title of the lot. Lifted from James T. Kirks original five-year mission statement yknow, the one about seeking out new life and new civilisations it conjures the spirit of adventure, that back-to-basics formula of an intrepid crew boldly going to unexplored regions of the galaxy. It has the potential to be the purest distillation of the original Star Trek ethos since The Next Generation last beamed off screens in 1994, and could just be just what the franchise and planet Earth needs in these unusual times.

Strange New Worlds certainly seems to be the show the Star Trek faithful want, with fan power a driving force in the series green light. Audiences were so taken with Captain Christopher Pike, Science Officer Spock and First Officer Number One when the USS Enterprise warped into Star Trek: Discovery last year that theyve been given the command codes to their own spin-off. Think Angel, Frasier or ahem Joey, but in the 23rd century.

When we said we heard the fans outpouring of love for Pike, Number One and Spock when they boardedStar Trek: Discoverylast season, we meant it, executive producer and Treks TV commander-in-chief Alex Kurtzman toldStarTrek.com. These iconic characters have a deep history in Star Trek canon, yet so much of their stories have yet to be told. The Enterprise, its crew and its fans are in for an extraordinary journey to new frontiers in the Star Trek universe.

Those frontiers arent entirely new, of course. Pike, Spock and Number One pre-date even Kirk himself, having headed up the Enterprise crew in the original Star Trek pilot. Filmed in 1965, their sole appearance in "The Cage" didnt make the grade with network executives and didnt air until decades later though the pilot did become canon via flashbacks in Original Series two-parter "The Menagerie". The suits had seen enough to give Star Trek creator Gene Roddenberry an unlikely second chance, but by the time the series left Spacedock in 1966, only Spock was still serving on the Enterprise bridge.

With barely an hour of screentime to play with, original Pike Jeffrey Hunter never really got the chance to make his mark. Indeed, despite his matinee idol good looks, Hunters Pike is too dry and strait-laced to convince as the lead of an action TV show there are few signs hed ever have become a pop culture icon of Kirk-shaped proportions.

Yet in just one season on board Discovery, Anson Mount turned Pike into one of Starfleets most memorable commanding officers, a man whose boy scout decency never got in the way of his innate charisma. The contrast with evil Mirror Universe CO Gabriel Lorca couldnt have been starker this Pike is so honourable that he takes painful visions of his tragic future on the chin for the greater good yet he instantly made the captains chair his own.

When Discovery blasted off to the distant future in the season two finale, established continuity ensured that Pike had to stay behind. So Strange New Worlds provides a welcome excuse to keep him and Spock and Number One on TV. Thats good news because Mount, Ethan Peck (as Spock) and Rebecca Romijn (as Number One a comparative blank slate at this point) have already done enough to suggest they have good enough on-screen chemistry to carry a show. Handled wisely the trio could even echo the iconic Kirk/Spock/McCoy axis that was the engine room of the Original Series.

If either Discovery or Picard were your introduction to the Star Trek universe, youll be wondering what executive producer Akiva Goldsman was on about when he told Variety, Were going to try to harken back to some classical Trek values, to be optimistic, and to be more episodic.

In Trek terms, however, the recent heavily serialised, morally ambiguous shows are the anomaly, as much products of the present day as the half-century-old franchise that spawned them. In this era of peak TV dominated by shades-of-grey antiheroes and complex moral choices Roddenberrys idealistic vision of the future had come to feel unfashionable, an anachronism of old-school network TV. But now that Trek has proved it can escape its roots, theres no reason it shouldnt go back why be apologetic about being part of one of the greatest pop culture franchises of all time?

Standalone stories of the week are part of Star Treks DNA. Beaming to a new planet, sorting out a few problems, going home and forgetting all about it that's been part of the mix since day one. But as with Doctor Who, the ability to be a new show every week, telling a different story in a different location with a new cast of supporting players, has always been key to Treks longevity. There are plenty of strange new worlds still to explore, and a hell of a lot of debates to have about the pro and cons of violating the Prime Directive. Who wants to let The Orville have all the fun?

Besides, theres no reason Spocks old adage about infinite diversity in infinite combinations shouldnt also apply to Star Trek TV shows. With Kurtzman having already told the Hollywood Reporter that, the intention is to have something Star Trek on the air all the time,Discovery, Picard and Strange New Worlds will be joined on screen by animated comedy Lower Decks and spy drama Section 31. That means even more Trek shows running simultaneously than we had in the glory days of the 90s and if theyre all going to survive, they need to be distinct.

(Image credit: Netflix)

... we have Star Trek: Discovery season 3 to look forward to. Click that link to find our everything we know about S3.

The powers-that-be (kind of) realised that in the 90s and early 00s Deep Space Nines space station setting was a big departure from The Next Generations starship adventures, while Voyagers lost in the Delta Quadrant set-up (theoretically) shook things up again. But DS9 aside those shows were often hamstrung by a What would Roddenberry do? approach that kept ongoing storylines and conflict between the ships crew at a bare minimum. Even Enterprise, set a century before the Original Series, struggled to break free from the franchises long-standing conventions. At least now there should be the freedom to have five shows all carving their unique course in the Star Trek universe. All Trek but all different.

Now that Discovery and Picard have pulled the franchise into the 21st century, the course is cleared for Strange New Worlds to celebrate Star Treks past, the modern-day franchises hymn to positivity. The depressing state of planet Earth right now doesnt mean that every TV show has to be a joyful celebration of life; therell always be room for complex drama exploring the dark side of the human condition. But the optimistic ideals of the future Trek was built on a world of tolerance, listening to other points of view, and working together towards a common goal are all messages we could use right now. If Star Trek cant work in that space unashamedly, then what on earth is it for?

Want more Trek coverage? Here's our guide to the Star Trek timeline

See more here:
Why Strange New Worlds is the show Star Trek and the world needs right now - GamesRadar+

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Animal Stem Cell Therapy Market What Factors will drive the Animal Stem Cell Therapy Market in Upcoming Years and How it is Going to Impact on Global...