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Archive for the ‘Biotechnology’ Category

AgeX Therapeutics and ImStem Biotechnology Sign Non-Binding Letter of Intent Regarding Investigational MSC Candidate IMS001 for COVID-19 and Other…

Thursday, June 4th, 2020

ALAMEDA, Calif. & FARMINGTON, Conn.--(BUSINESS WIRE)--AgeX Therapeutics, Inc. (AgeX: NYSE American: AGE), a biotechnology company developing therapeutics for human aging and regeneration, and ImStem Biotechnology, Inc., a biopharmaceutical company developing human embryonic stem cell-derived mesenchymal stem cells (hES-MSC), today announced their signing of a non-binding letter of intent for ImStem to obtain from AgeX a non-exclusive license to use AgeXs embryonic stem cell line ESI 053 to derive ImStems investigational MSC product IMS001 for development in COVID-19 as well as acute respiratory distress syndrome (ARDS) due to other causes. AgeX and ImStem are co-operating to finalize financial terms and other provisions of a license agreement.

ImStem has previously used AgeX ESI 053 to derive the ImStem IMS001 product which is being investigated for multiple sclerosis under an IND. Earlier this year, the U.S. Food and Drug Administration (FDA) cleared IMS001 to begin a Phase 1 clinical study in patients with multiple sclerosis, after a clinical hold on its Investigational New Drug (IND) application was removed. This is believed to be the first MSC product derived from human embryonic stem cells to be accepted for a clinical trial by the FDA. AgeX and ImStem already have a commercial license in place, which grants ImStem rights to use AgeXs ESI 053 to derive IMS001 as a product candidate for development in autoimmune disease, including multiple sclerosis.

To date, in patients with pneumonia and ARDS due to COVID-19, preliminary literature suggests MSCs, such as ImStems hES-MSC candidate IMS001, may warrant further development consideration. An early clinical study conducted in China by an unrelated group with a different MSC product, Transplantation of ACE2- Mesenchymal Stem Cells Improves the Outcome of Patients with COVID-19 Pneumonia, and published in Aging and Disease (2020, Vol. 11, No. 2, pp. 216-228) showed that an intravenous infusion of a different MSC product appeared safe and improved functional outcomes in seven treated patients with COVID-19 pneumonia. MSCs are well recognized to be immunomodulatory in nature, possessing immunosuppressive and anti-inflammatory properties.

Even before their application to COVID-19, MSCs were being investigated as a potential therapeutic option in ARDS, and emerging data in preclinical models has been encouraging. ARDS remains an area of considerable unmet medical need, affecting around 200,000 patients annually in the U.S., accounting for 10% of all intensive care unit patients, and having a mortality of approximately 40%. At the present time, no specific direct therapies exist for ARDS and only supportive treatment is available.

We feel privileged to be part of a global effort to combat COVID-19. This is a unique opportunity for AgeX to leverage its resources to help with the public health challenge at hand. Decades of pioneering work with human embryonic stem cells means this technology is now at a point where it may play a role in the development of a cell-based approach to combating COVID-19. We are very excited by the prospect of expanding our relationship with ImStem to include COVID-19 and ARDS, said Dr. Nafees Malik, Chief Operating Officer of AgeX.

We welcome the opportunity to continue to collaborate with AgeX and explore future development of our IMS001 product in COVID-19 and ARDS from other causes, commented Richard Kim, M.D., Chief Medical Officer of ImStem Biotechnology.

About AgeX Therapeutics

AgeX Therapeutics, Inc. (NYSE American: AGE) is focused on developing and commercializing innovative therapeutics for human aging. AgeXs PureStem and UniverCyte manufacturing and immunotolerance technologies are designed to work together to generate highly defined, universal, allogeneic, off-the-shelf pluripotent stem cell-derived young cells of any type for application in a variety of diseases with a high unmet medical need. AgeX has two preclinical cell therapy programs: AGEX-VASC1 (vascular progenitor cells) for tissue ischemia and AGEX-BAT1 (brown fat cells) for Type II diabetes. AgeXs revolutionary longevity platform induced Tissue Regeneration (iTR) aims to unlock cellular immortality and regenerative capacity to reverse age-related changes within tissues. AGEX-iTR1547 is an iTR-based formulation in preclinical development. HyStem is AgeXs delivery technology to stably engraft PureStem cell therapies in the body. AgeXs core product pipeline is intended to extend human healthspan. AgeX is seeking opportunities to establish licensing and collaboration arrangements around its broad IP estate and proprietary technology platforms and therapy product candidates.

For more information, please visit http://www.agexinc.com or connect with the company on Twitter, LinkedIn, Facebook, and YouTube.

About ImStem Biotechnology

ImStem Biotechnology, Inc. is aspiring to revolutionize how serious diseases with significant unmet needs are treated with a new generation of regenerative and cellular therapies. Pioneering research by its current founder and Chief Technology Officer Dr. Xiaofang Wang and Dr. Ren-He Xu, former director of UConn Stem Cell Institute, led to the proprietary state-of-the-art pluripotent stem cell technology, enabling off-the-shelf, allogeneic stem cell-derived products to be manufactured in scale, differentiating itself from the typical challenges imposed by autologous adult cell therapy products. The company's mission is to advance the science and understanding of human pluripotent stem cell based regenerative cellular therapies through novel and creative development pathways and to fulfill unmet medical needs in serious diseases. And its development strategy focuses on neurologic, autoimmune, degenerative, and rare orphan diseases. ImStem Biotechnology Inc. is a privately held company headquartered in Farmington, CT.

For more information, visit http://www.imstem.com.

Forward-Looking Statements for AgeX

Certain statements contained in this release are forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Any statements that are not historical fact including, but not limited to statements that contain words such as will, believes, plans, anticipates, expects, estimates should also be considered forward-looking statements. Forward-looking statements involve risks and uncertainties. Actual results may differ materially from the results anticipated in these forward-looking statements and as such should be evaluated together with the many uncertainties that affect the business of AgeX Therapeutics, Inc. and its subsidiaries, particularly those mentioned in the cautionary statements found in more detail in the Risk Factors section of AgeXs most recent Annual Report on Form 10-K and Quarterly Report on Form 10-Q filed with the Securities and Exchange Commissions (copies of which may be obtained at http://www.sec.gov). Subsequent events and developments may cause these forward-looking statements to change. In addition, with respect to AgeXs letter of intent with ImStem there is no assurance that (i) AgeX and ImStem will successfully conclude negotiations and enter into a license agreement; (ii) ImStem will be successful in developing any therapeutic products from a stem cell line licensed by AgeX or that any therapeutic product that may be developed will receive FDA or foreign regulatory approval, or (iii) AgeX will derive revenue or other financial benefits from any license agreement that might be signed with ImStem. AgeX specifically disclaims any obligation or intention to update or revise these forward-looking statements as a result of changed events or circumstances that occur after the date of this release, except as required by applicable law.

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AgeX Therapeutics and ImStem Biotechnology Sign Non-Binding Letter of Intent Regarding Investigational MSC Candidate IMS001 for COVID-19 and Other...

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AgeX Therapeutics, ImStem Biotechnology sign non-binding letter of intent regarding investigational MSC candidate IMS001 for Covid-19 – Pharmaceutical…

Thursday, June 4th, 2020

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AgeX Therapeutics, ImStem Biotechnology sign non-binding letter of intent regarding investigational MSC candidate IMS001 for Covid-19 - Pharmaceutical...

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Biotechnology Reagents Market Analysis and Technology Advancement Outlook 2020 to 2025 – Cole of Duty

Thursday, June 4th, 2020

The report presents an in-depth assessment of the Biotechnology Reagents Market including enabling technologies, key trends, market drivers, challenges, standardization, regulatory landscape, deployment models, operator case studies, opportunities, future roadmap, value chain, ecosystem player profiles and strategies. The report also presents forecasts for Biotechnology Reagents investments from 2020 till 2026.

Global biotechnology reagents market is expected to rise from its initial estimated value of USD 65.82 billion in 2018 to an estimated value of USD 118.53 billion by 2026, registering a CAGR of 7.63% in the forecast period of 2019-2026.

Click the link to get a Sample Copy of the Report:

https://www.marketinsightsreports.com/reports/11191577929/global-biotechnology-reagents-market-professional-survey-report-2019/inquiry?source=coleofduty&Mode=48

The report presents the market competitive landscape and a corresponding detailed analysis of the major vendor/key players in the market. Top Companies in the Global Biotechnology Reagents Market: Agilent Technologies, Thermo Fisher Scientific, SGS, Shimadzu, Waters, Charles River Laboratories, Bioinformatics Solutions, Proteome Factory, Rapid Novor, Selvita

Biotechnology reagents are substances or compounds used to detect or synthesize another substance in order to give a reading test. These reagents are used in the field of research, genetics, molecular biology, diagnosis, immunology and bioscience. Biotechnology reagent consists of technologies such as cell culture, spectrometry, IVD, PCR, chromatography, expression and transfection, flow cytometer, and electrophoresis, and finds their application in various fields such as the immune phenotype, fluorescent microscopy, DNA analysis and cell cycle analysis.

This report segments on the basis of Types:

Life Science ReagentsAnalytical Reagents

Split On the basis of Applications:

Protein Synthesis and PurificationGene ExpressionDNA and RNA AnalysisDrug Testing

Inquire for Discount:

https://www.marketinsightsreports.com/reports/11191577929/global-biotechnology-reagents-market-professional-survey-report-2019/discount?source=coleofduty&Mode=48

Regional Analysis:

For comprehensive understanding of market dynamics, the global Biotechnology Reagents Market is analysed across key geographies namely: United States, China, Europe, Japan, South-east Asia, India and others. Each of these regions is analysed on basis of market findings across major countries in these regions for a macro-level understanding of the market.

Influence of the Biotechnology Reagents Market report:

-Comprehensive assessment of all opportunities and risk in the Biotechnology Reagents Market.

-Biotechnology Reagents Market recent innovations and major events.

-Detailed study of business strategies for growth of the Biotechnology Reagents Market-leading players.

-Conclusive study about the growth plot of Biotechnology Reagents Market for forthcoming years.

-In-depth understanding of Biotechnology Reagents Market-particular drivers, constraints and major micro markets.

-Favourable impression inside vital technological and market latest trends striking the Biotechnology Reagents Market.

The report has 150 tables and figures browse the report description and TOC:

https://www.marketinsightsreports.com/reports/11191577929/global-biotechnology-reagents-market-professional-survey-report-2019?source=coleofduty&Mode=48

What are the market factors that are explained in the report?

Key Strategic Developments: The study also includes the key strategic developments of the market, comprising R&D, new product launch, M&A, agreements, collaborations, partnerships, joint ventures, and regional growth of the leading competitors operating in the market on a global and regional scale.

Key Market Features: The report evaluated key market features, including revenue, price, capacity, capacity utilization rate, gross, production, production rate, consumption, import/export, supply/demand, cost, market share, CAGR, and gross margin. In addition, the study offers a comprehensive study of the key market dynamics and their latest trends, along with pertinent market segments and sub-segments.

Analytical Tools: The Global Biotechnology Reagents Market report includes the accurately studied and assessed data of the key industry players and their scope in the market by means of a number of analytical tools. The analytical tools such as Porters five forces analysis, feasibility study, and investment return analysis have been used to analysed the growth of the key players operating in the market.

Finally, Biotechnology Reagents Market report is the believable source for gaining the Market research that will exponentially accelerate your business. The report gives the principle locale, economic situations with the item value, benefit, limit, generation, supply, request and Market development rate and figure and so on. This report additionally Present new task SWOT examination, speculation attainability investigation, and venture return investigation.

Note: All the reports that we list have been tracking the impact of COVID-19. Both upstream and downstream of the entire supply chain has been accounted for while doing this. Also, where possible, we will provide an additional COVID-19 update supplement/report to the report in Q3, please check for with the sales team.

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Vir Biotechnology Is Bucking The Biotech COVID-19 Trends, And Stands To Win – Motley Fool

Thursday, June 4th, 2020

Thanks to its newly announced COVID-19 antibody therapy candidates, Vir Biotechnology's (NASDAQ:VIR) stock is still up more than 10% from the beginning of May and more than 180% from the start of the year.On top of its recent gains, there's reason to believe that Vir is positioned perfectly for continued growth.

While the company has a long way to go before it reaches profitability, between its low-risk pipeline programs for COVID-19 and a demonstrated competency for preclinical drug development for infectious disease, Vir's future seems bright.

Image source: Getty Images.

Vir's preclinical COVID-19 projects include two antibody therapies that it claims could temporary prevention and the treatment of coronavirus infections. VIR-7832 is both a prophylactic and a therapeutic, whereas VIR-7831 is only a therapeutic.

Because they are antibody therapies, Vir's candidates would be more effective at helping sick patients get better by reducing their viral load than it would be at preventing infections like a traditional vaccine might. In a nutshell, both of Vir's antibody programs could help patients to fight COVID-19 immediately by neutralizing viral particles in their bloodstream after they get a dose of the therapy. Then, once the patient's symptoms subside, the antibodies would remain in their system for several days or weeks, protecting them from re-infection. This process is key to both of Vir's COVID-19 antibody programs, but there's a bit more to the story.

Vir suspects that VIR-7832 may also function as a T-cell vaccine, training the immune system to react to future infections. This would mean that patients could be administered the antibody even if they don't expect to get sick. If Vir's hunch is correct, VIR-7832 would provide longer-lasting immunity than VIR-7831, and it might be a contender for mass production as a prophylactic.

The company's approach is uncontroversial from a scientific perspective, given that neutralizing antibodies from COVID-19 survivors have already been shown to combat the disease in vitro by numerous independent research teams and similar therapies were successfully used to treat human patients with SARS. Similarly, Vir's approach is front-run by ongoing clinical trials testing the efficacy of antibodies from recovered COVID-19 patients on improving disease outcomes in people who are currently ill.

The average vaccine in development is estimated to have only a 6% chance of proceeding all the way to approval and the market, but Vir's antibody products may fare better because they are adapted from natural antibodies known to be effective and safe. There's no guarantee of Vir's efforts ending in blockbuster revenue, but in the highly risky world of biotech, the prospects of these two COVID-19 projects are extremely favorable even from a conservative perspective.

However, given that the antibodies would be copies of naturally ocurring antibodies, it's uncertain whether intellectual property protection would be sufficient to prevent a competitor from creating very similar products. For most biotech companies, this would be a dealbreaker, as it would effectively prevent the ability to recoup development costs with a period of exclusive production rights. But not for Vir. By bucking the traditional wisdom regarding exclusivity and drug development, Vir has a real chance of entering the market sooner than competitors at a time when demand for its product would be enormously high.

That isn't to say that Vir is an unambitious company because it is moving forward with safer programs. In contrast to its two antibody therapy programs, Vir's VIR-2703 program is riskier because it uses a scientific approach which hasn't been tested in humans for the purpose of infectious disease. Rather than acting to neutralize viral particles directly like an antibody might, VIR-2703 relies on small chunks of genetic information called silencing RNAs (siRNAs) which disrupt regions of the viral genome.

Counting on this program to succeed would be a mistake. Most large pharmaceutical companies gave up trying to develop siRNA therapies in the mid-2010s after nearly a decade of failures, and the only siRNA therapy approved by the FDA isn't for an infectious disease.

On the other hand, early favorable clinical results from VIR-2703 should not be interpreted as a reason to buy the company's stock. Stumbles stemming from a lack of a proof of concept in human patients further down the pipeline could easily erase any gains. Either way, Vir's drug development pipeline looks more like a risk-balanced portfolio than a selection of technological and scientific gambles like so many other biotechs.

If Vir brings one of its COVID-19 programs to market, it'll be one more addition to the company's impressive roster of therapies and prophylactics for viral diseases. Aside from its three unique COVID-19 programs, Vir's pipeline includes a handful of other projects intended to treat or prevent illnesses caused by hepatitis B, influenza, tuberculosis, and even HIV. Importantly, all but two of these pipeline projects are in the preclinical phase, so the company's clinical acumen is far from proven.

In terms of advanced programs, the closest Vir has to offer is its VIR-2218 therapy for hepatitis B, which it suspects may be curative for most patients. If Vir brings a curative therapy to market, the company may have trouble maintaining its revenue over the long term because a cure shrinks the pool of eligible patients. As the hepatitis B therapeutics market is only worth around $2.6 billion, it's possible that Vir's hepatitis B therapy would meet the same fate as the low-earning hepatitis C therapy produced by Gilead Sciences (NASDAQ:GILD)But, with 257 million people worldwide living with hepatitis B compared to only 71 million living with hepatitis C, it's less likely that Vir will experience the same difficulties. Importantly, Vir isn't letting Gilead's experience stop them from moving forward with a curative therapy candidate. Even if the long-term profitability of VIR-2218 is in jeopardy of being a victim of its own success, Vir is willing to take a chance rather than stick to a safer opportunity.

In summary, Vir's COVID-19 pipeline has two antibody programs that have a better than average chance of passing through clinical trials.Elsewhere, the company's technology platform appears formidable, but its clinical pipeline is still in its infancy, despite a bevy of compelling seedlings.

Given the level of public need for COVID-19 treatments and vaccines, it's likely that if Vir's COVID-19 programs look promising once they hit the clinic in the summer, they'll be expedited through clinical trials. This means that the company's minimal past experience in clinical operations and clinical development will be of little use, so it's likely to need to lean heavily on larger collaborators like Biogen, GlaxoSmithKline, and Alnylam Pharmaceuticals.

It's easy to envision a future where Vir gets acquired by one of these collaborators if its trials have positive outcomes. In the meantime, progress by Vir's major competitors like Novavax and behemoth vaccine producers like Merck is unlikely to diminish the company's upward trajectory, as competing products would be targeted at preventing COVID-19 rather than both treating and preventing it.

Image Source: YCharts

As the market grows to recognize Vir as a rising contender in the COVID-19 therapeutic market, public interest in the company will explode, to the benefit of its shareholders. I'd recommend buying Vir shares now, to maximize the benefit of successive boosts to the company's stock price as its COVID-19 candidates pass through each phase of clinical trials. Holding onto Vir for a few years will maximize the gains, but don't discount the probability of near-term gains either.

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Outlook on the Worldwide Biotechnology Reagents Industry to 2027 – Agreements, Partnerships and Collaborations & Joint Ventures – Yahoo Finance

Thursday, June 4th, 2020

Dublin, June 02, 2020 (GLOBE NEWSWIRE) -- The "Biotechnology Reagents - Global Market Outlook (2018-2027)" report has been added to ResearchAndMarkets.com's offering.

The Global Biotechnology Reagents market accounted for $69.21 billion in 2018 and is expected to reach $163.19 billion by 2027 growing at a CAGR of 10.0% during the forecast period. Rising number of biotechnology firms and growth in biopharmaceuticals are the major factors propelling the market growth. However, high cost of reagents is hampering the market growth.

Biotechnology reagents are the substances used to detect or synthesize another substance so as to provide a test reading. The biotechnological reagents play an important role in the age of rapid research, discovery, and publication in the industry and academic research purposes.

Based on the technology, the analytical segment is going to have a lucrative growth during the forecast period as chromatography technique of analytical technology is mostly used in drug discovery to validate the specificity, sensitivity, and purity of drugs and deliver precise outcomes to validate characters. By geography, North America is going to have a lucrative growth during the forecast period owing to high investments, new product developments, presence of favorable government policies and sophisticated healthcare infrastructure.

Some of the key players profiled in the Biotechnology Reagents Market include Siemens Healthineers, Quality Biological Inc., Merck Millipore, PerkinElmer, Meridian Bioscience, Promega Corporation, Lonza Group AG, BioMrieux, GE Healthcare, Bio-Rad Laboratories, Life Technologies, Beckman Coulter, Agilent Technologies, Abbott Laboratories and Becton Dickinson.

What our report offers:

Key Topics Covered:

1 Executive Summary

2 Preface2.1 Abstract 2.2 Stake Holders 2.3 Research Scope 2.4 Research Methodology2.4.1 Data Mining2.4.2 Data Analysis2.4.3 Data Validation2.4.4 Research Approach2.5 Research Sources 2.5.1 Primary Research Sources 2.5.2 Secondary Research Sources 2.5.3 Assumptions

3 Market Trend Analysis3.1 Introduction 3.2 Drivers 3.3 Restraints 3.4 Opportunities 3.5 Threats 3.6 Technology Analysis 3.7 Application Analysis 3.8 End User Analysis 3.9 Emerging Markets 3.10 Impact of Covid-19

4 Porters Five Force Analysis

5 Global Biotechnology Reagents Market, By Technology5.1 Introduction 5.2 Life Science 5.2.1 Polymerase Chain Reaction 5.2.1.1 Master Mixes 5.2.1.2 Kits5.2.1.3 Individual Reagent 5.2.2 Cell/Tissue Culture5.2.2.1 Sera5.2.2.2 Media and Regents 5.2.3 In-Vitro Diagnostics5.2.3.1 Microbiology Culture 5.2.3.2 Hematology 5.2.3.3 Immunoassay 5.2.3.4 Clinical Chemistry 5.2.3.5 Molecular Diagnostics 5.2.4 Expression and Transfection 5.3 Analytical 5.3.1 Chromatography5.3.1.1 Super Critical Fluid Chromatography5.3.1.2 Liquid Chromatography 5.3.1.3 Ion Chromatography 5.3.1.4 Gas Chromatography 5.3.1.5 Reagents Type 5.3.1.5.1 Solvent 5.3.1.5.2 Chemical 5.3.1.5.3 Adsorbents 5.3.2 Mass Spectrometry5.3.2.1 Proteomics 5.3.2.2 Drug Discovery 5.3.2.3 Clinical Testing 5.3.2.4 Genomics5.3.3 Electrophoresis5.3.3.1 Gel5.3.3.2 Dye5.3.3.3 Buffer5.3.4 Flow Cytometry5.3.4.1 Cell-based Flow Cytometry 5.3.4.2 Bead-based Flow Cytometry

6 Global Biotechnology Reagents Market, By Application6.1 Introduction 6.2 Protein Synthesis and Purification 6.3 Immunophenotyping 6.4 Gene Expression 6.5 Fluorescent Microscopy6.6 Drug testing 6.7 DNA and RNA analysis6.8 Cell Cycle Analysis

7 Global Biotechnology Reagents Market, By End User7.1 Introduction 7.2 Research Institutes 7.3 Pharmaceuticals 7.4 Diagnostic Centers 7.5 Biotech Companies

8 Global Biotechnology Reagents Market, By Geography8.1 Introduction 8.2 North America 8.2.1 US 8.2.2 Canada 8.2.3 Mexico 8.3 Europe 8.3.1 Germany 8.3.2 UK 8.3.3 Italy 8.3.4 France 8.3.5 Spain 8.3.6 Rest of Europe8.4 Asia Pacific 8.4.1 Japan 8.4.2 China 8.4.3 India 8.4.4 Australia 8.4.5 New Zealand8.4.6 South Korea8.4.7 Rest of Asia Pacific8.5 South America 8.5.1 Argentina 8.5.2 Brazil 8.5.3 Chile 8.5.4 Rest of South America 8.6 Middle East & Africa 8.6.1 Saudi Arabia8.6.2 UAE 8.6.3 Qatar 8.6.4 South Africa8.6.5 Rest of Middle East & Africa

9 Key Developments9.1 Agreements, Partnerships, Collaborations and Joint Ventures9.2 Acquisitions & Mergers9.3 New Product Launch 9.4 Expansions 9.5 Other Key Strategies

10 Company Profiling10.1 Siemens Healthineers10.2 Quality Biological Inc.10.3 Merck Millipore 10.4 PerkinElmer 10.5 Meridian Bioscience 10.6 Promega Corporation10.7 Lonza Group AG 10.8 BioMrieux 10.9 GE Healthcare 10.10 Bio-Rad Laboratories10.11 Life Technologies 10.12 Beckman Coulter 10.13 Agilent Technologies 10.14 Abbott Laboratories 10.15 Becton Dickinson

For more information about this report visit https://www.researchandmarkets.com/r/y9konb

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Research on Media, Sera and Reagents in Biotechnology Market (impact of COVID-19) with Top Players: Athena Environmental Science, Inc., Becton,…

Thursday, June 4th, 2020

Global Media, Sera and Reagents in Biotechnology Market: Trends Estimates High Demand by 2027

The Media, Sera and Reagents in Biotechnology Market 2020 report includes the market strategy, market orientation, expert opinion and knowledgeable information. The Media, Sera and Reagents in Biotechnology Industry Report is an in-depth study analyzing the current state of the Media, Sera and Reagents in Biotechnology Market. It provides a brief overview of the market focusing on definitions, classifications, product specifications, manufacturing processes, cost structures, market segmentation, end-use applications and industry chain analysis. The study on Media, Sera and Reagents in Biotechnology Market provides analysis of market covering the industry trends, recent developments in the market and competitive landscape.

It takes into account the CAGR, value, volume, revenue, production, consumption, sales, manufacturing cost, prices, and other key factors related to the global Media, Sera and Reagents in Biotechnology market. All findings and data on the global Media, Sera and Reagents in Biotechnology market provided in the report are calculated, gathered, and verified using advanced and reliable primary and secondary research sources. The regional analysis offered in the report will help you to identify key opportunities of the global Media, Sera and Reagents in Biotechnology market available in different regions and countries.

The final report will add the analysis of the Impact of Covid-19 in this report Media, Sera and Reagents in Biotechnology industry.

Some of The Companies Competing in The Media, Sera and Reagents in Biotechnology Market are: Athena Environmental Science, Inc., Becton, Dickinson, CellGenix, GE Healthcare, Lonza, Thermo Fisher Scientific, Inc., and

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The report scrutinizes different business approaches and frameworks that pave the way for success in businesses. The report used Porters five techniques for analyzing the Media, Sera and Reagents in Biotechnology Market; it also offers the examination of the global market. To make the report more potent and easy to understand, it consists of info graphics and diagrams. Furthermore, it has different policies and improvement plans which are presented in summary. It analyzes the technical barriers, other issues, and cost-effectiveness affecting the market.

Global Media, Sera and Reagents in Biotechnology Market Research Report 2020 carries in-depth case studies on the various countries which are involved in the Media, Sera and Reagents in Biotechnology market. The report is segmented according to usage wherever applicable and the report offers all this information for all major countries and associations. It offers an analysis of the technical barriers, other issues, and cost-effectiveness affecting the market. Important contents analyzed and discussed in the report include market size, operation situation, and current & future development trends of the market, market segments, business development, and consumption tendencies. Moreover, the report includes the list of major companies/competitors and their competition data that helps the user to determine their current position in the market and take corrective measures to maintain or increase their share holds.

What questions does the Media, Sera and Reagents in Biotechnology market report answer pertaining to the regional reach of the industry?

The report claims to split the regional scope of the Media, Sera and Reagents in Biotechnology market into North America, Europe, Asia-Pacific, South America & Middle East and Africa. Which among these regions has been touted to amass the largest market share over the anticipated duration

How do the sales figures look at present how does the sales scenario look for the future?

Considering the present scenario, how much revenue will each region attain by the end of the forecast period?

How much is the market share that each of these regions has accumulated presently

How much is the growth rate that each topography will depict over the predicted timeline

A short overview of the Media, Sera and Reagents in Biotechnology market scope:

Global market remuneration

Overall projected growth rate

Industry trends

Competitive scope

Product range

Application landscape

Supplier analysis

Marketing channel trends Now and later

Sales channel evaluation

Market Competition Trend

Market Concentration Rate

Reasons to Read this Report

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:

Chapter 1:Media, Sera and Reagents in Biotechnology Market Overview

Chapter 2: Global Economic Impact on Industry

Chapter 3:Media, Sera and Reagents in Biotechnology Market Competition by Manufacturers

Chapter 4: Global Production, Revenue (Value) by Region

Chapter 5: Global Supply (Production), Consumption, Export, Import by Regions

Chapter 6: Global Production, Revenue (Value), Price Trend by Type

Chapter 7: Global Market Analysis by Application

Chapter 8: Manufacturing Cost Analysis

Chapter 9: Industrial Chain, Sourcing Strategy and Downstream Buyers

Chapter 10: Marketing Strategy Analysis, Distributors/Traders

Chapter 11: Media, Sera and Reagents in Biotechnology Market Effect Factors Analysis

Chapter 12: GlobalMedia, Sera and Reagents in Biotechnology Market Forecast to 2027

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Nanoparticles in Biotechnology and Pharmaceuticals Market Key Players, SWOT Analysis, Dynamics, Drivers, Key Indicators and Forecast to 2026 – Farmers…

Thursday, June 4th, 2020

The report is one of the most comprehensive and accurate research studies on the Nanoparticles in Biotechnology and Pharmaceuticals Market. Sheds light on market competition, segmentation, regional growth, and dynamics, such as drivers, constraints, trends, and opportunities. It provides validated and revalidated market figures, which include market size, CAGR, market share, revenue, gross margin, production, and consumption. It offers absolute dollar opportunity analysis, manufacturing cost analysis, Porters five-force analysis, qualitative and quantitative analysis, and PESTLE analysis to provide a complete understanding of the Nanoparticles in Biotechnology and Pharmaceuticals market. It is prepared with the use of the best techniques and tools for primary and secondary research.

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Top 10 Companies in the Nanoparticles in Biotechnology and Pharmaceuticals Market Research Report:

The regional analysis provided in the report helps to familiarize yourself with the growth opportunities available in different regions and countries around the world. Provides market share, consumption, production, income, and other important geographic market research. The competitive analysis includes the company profile of the main players based on recent developments, revenue, gross margin and other key factors. The report offers useful recommendations for players to secure a solid position in the Nanoparticles in Biotechnology and Pharmaceuticals market. It comes as a powerful set of guidelines to prepare for unforeseen challenges and ensure healthy growth in the Nanoparticles in Biotechnology and Pharmaceuticals market.

Table of Contents

Market Overview: Offers a broad product scope and Nanoparticles in Biotechnology and Pharmaceuticals market overview followed by a look at the segmentation study provided in the report. For product segments, it offers production and growth rate comparisons followed by production market shares, and for application segments, it offers a deep consumption comparison. For regional segments, it provides comparisons of market size and growth rate for the 2013-2025 review period. It also includes the perspective of the size of the global market, taking into account production and income.

Manufacturers Competition Here, manufacturers production, earnings, and average price are studied alongside their stocks. In addition, manufacturers products and manufacturing base distribution are discussed in this section, followed by competitive situations and trends.

Production by region: This section highlights global capacity, production and income and their market shares by region, followed by analysis of prices and gross margin. Each regional market studied in the report is analyzed in terms of production, growth rate, income, price, production, capacity and gross margin.

Manufacturing Cost Analysis: In this part of the report, analysts have focused on the analysis of key raw materials, the proportion of the manufacturing cost structure, and the analysis of manufacturing processes. Under the analysis of key raw materials, they discussed the key raw materials, their price trend, their suppliers and their market concentration rate. Under the proportion of the manufacturing cost structure, they have concentrated on raw materials and labor costs.

Global Market Forecast: The global market forecast includes a detailed perspective of capacity, production, revenue, growth rate, and price trend. This section also provides a forecast of all the regional markets studied in the report based on production, income, consumption and price.

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The main questions our analysts have addressed

What policies and regulations will have a major impact on the global market?What are the current and future opportunities in the global market?What will be the size of the global market in the next five years?What are the important dynamics of the market?

Research Methodology

Competitive scene

The main objectives of the report

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Our 250 Analysts and SMEs offer a high level of expertise in data collection and governance use industrial techniques to collect and analyse data on more than 15,000 high impact and niche markets. Our analysts are trained to combine modern data collection techniques, superior research methodology, expertise and years of collective experience to produce informative and accurate research.

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The Daily Biotech Pulse: FDA Nod For Roche’s Combo Therapy In Liver Cancer, Allena Rips Higher, Pfizer To Invest Up To $500M In Biotechs – Benzinga

Thursday, June 4th, 2020

Here's a roundup of top developments in the biotech space over the last 24 hours:

(Biotech Stocks Hitting 52-week Highs June 1)

(Biotech Stocks Hitting 52-week Lows June 1)

Roche Holdings AG Basel ADR Common Stock (OTC: RHHBY) said the FDA approved its Tecentriq in combination with Avastin for the treatment of people with unresectable or metastatic hepatocellular carcinoma who have not received prior systemic therapy.

Allena Pharmaceuticals Inc (NASDAQ: ALNA) shares were surging ahead of the company's presentation at the Jefferies Virtual Healthcare Conference. The shares were higher in Monday's regular session, reacting to an initiation by H.C. Wainwright with a Buy rating and $10 price target.

Analyst Edward White said the biopharma is an "undervalued enzyme therapeutic company."

Following a 31.55% jump to $2.21 in Monday's regular session, Allena shares were rallying by 35.29% to $2.99 in Tuesday's premarket session.

Esperion Therapeutics Inc (NASDAQ: ESPR) shares came under pressure after a federal district court accorded class action status to a lawsuit filed on behalf of investors, alleging the company issued misleading statements about its non-statin cholesterol-lowering drug Nexletol in a bid to artificially inflate thestock price.

The stock fell after it was evident the drug did not have a clear path to regulatory approval, the lawsuit alleged.

The stock slid 3.07% to $40.77 in after-hours trading.

Related Link:The Week Ahead In Biotech: ASCO, Menlo And Merck FDA Decisions, IPOs In The Spotlight

Pfizer Inc. (NYSE: PFE) announced the establishment of the Pfizer Breakthrough Growth Initiative, through which the company said itwill invest up to $500 million in biotechnology companies to help provide funding and access to its scientific expertise to ensure continuity of the biotechnology companies' most promising clinical development programs.

Sumitovant Biopharma said its affiliate Myovant Sciences Ltd (NYSE: MYOV) has submitted an NDA for the once-daily relugolix combo tablet, comprising relugolix 40 mg, estradiol 1mg and norethindrone acetate 0.5 mg, for the treatment of women with heavy menstrual bleeding associated with uterine fibroids.

The stock was trading 0.95% higher at $17.09 in the premarket session.

Sanofi SA (NASDAQ: SNY) said the European Commission has approved its Sarclisain combination with pomalidomide and dexamethasone for the treatment of adult patients with relapsed and refractory multiple myeloma who have received at least two prior therapies including lenalidomide and a proteasome inhibitor and have demonstrated disease progression on the last therapy.

Aytu Bioscience Inc (NASDAQ: AYTU) said it has retired $15 million debt assumed in connection with its previously announced acquisition of Cerecor Inc's(NASDAQ: CERC) Commercial Portfolio.

Tetraphase Pharmaceuticals Inc (NASDAQ: TTPH) said a revised offer from Melinta received in response to another revised offer from anothersuitor,AcelRx Pharmaceuticals Inc (NASDAQ: ACRX), has been deemed a superior offer by its board.

Melinta and AcelRx have been engaged in a bidding war to lap up Tetraphase, with both companies sweetening their respective bids a few times.

The revised AcelRx offer received May 27 called for exchanging each unit ofTetraphase stock for $0.5872 in cash and 0.7409AcelRx shares, representing $1.70 in upfront per share value, and one CVR, entitling the holders to receive potential payments of up to $16 million in cash upon the achievement of certain future Xerava net sales milestones starting in 2021.

Melinta's most recent bid offered $39 million in cash,plus an additional $16 million in cash potentially payable under CVR to be issued in the proposed acquisition.

In premarket trading Tuesday, Tetraphase gained 6.9% to $2.48, while AcelRx shares were surging higher by 6.3% to $1.35.

OraSure Technologies, Inc. (NASDAQ: OSUR) said it has commenced an underwritten public offering of 8 million shares of its common stock.

The stock slipped 4.32% to $13.51 in after-hours trading.

Adaptimmune priced its underwritten public offering of 20.5 million shares of its ADSs at $11 eachfor gross proceeds of $225.5 million. The company expects the offering to close on or about June 4.

Kaleido Biosciences Inc (NASDAQ: KLDO) priced its underwritten public offering of 4.75 million shares of its common stock at $7.50 per share. The company expects to raise gross proceeds of $35.6 million from the offering. All the shares are being offered by the company. The offering is expected to close June 4.

The stock was trading 2.87% higher at $8.24 in the premarket session.

Allogene Therapeutics Inc (NASDAQ: ALLO) priced its underwritten public offering of 11.702 million shares at $47 per share for gross proceeds of $550 million.The offering is expected to close on or about June 4.

The stock fell 0.57% to $48.66 in after-hours trading.

Guardant Health Inc (NASDAQ: GH) announced the commencement of a proposed underwritten public offering of 10 million shares of its common stock, of which 3 million shares are being offered by Guardant Health and 7 million by SoftBank Investment.

The stock was up 0.1% at $48.99 premarket.

G1 Therapeutics Inc (NASDAQ: GTHX) said it has entered into a debt financing agreement with Hercules Capital, Inc. (NYSE: HTGC) for up to $100 million. The company plans to use the proceeds to fund commercialization and further development of trilaciclib, its first-in-class investigational therapy designed to improve outcomes for people with cancer treated with chemotherapy.

Intellia Therapeutics Inc (NASDAQ: NTLA) said it has commenced an underwritten public offering of $75 million of shares of its common stock. All of the shares in the proposed offering are to be sold by Intellia.

Intellia shares were trading 0.91% higher at $20.73 premarket Tuesday.

Related Link: Attention Biotech Investors: Mark Your Calendar For June PDUFA Dates

2020 Benzinga.com. Benzinga does not provide investment advice. All rights reserved.

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The Daily Biotech Pulse: FDA Nod For Roche's Combo Therapy In Liver Cancer, Allena Rips Higher, Pfizer To Invest Up To $500M In Biotechs - Benzinga

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COVID-19 Update: Global Biotechnology Market is Expected to Grow at a Healthy CAGR with Top players: Johnson & Johnson, Roche, Pfizer, Merck,…

Thursday, June 4th, 2020

Global Biotechnology Market Report is a professional and in-depth research report on the worlds major regional market. The Biotechnology industry2020 by Industry Demand, Business Strategy & Emerging Trends by Leading Players. The Global pandemic of COVID19/CORONA Virus calls for redefining of business strategies. This Biotechnology Market report includes the impact analysis necessary for the same.

Download the Sample ToC to understand the CORONA Virus/COVID19 impact and be smart in redefining business strategies. https://inforgrowth.com/CovidImpact-Request/6321901/biotechnology-market

Top Players Listed in the Biotechnology Market Report areJohnson & Johnson, Roche, Pfizer, Merck, Sanofi, AstraZeneca, Gilead, CELGENE CORPORATION, Biogen, Amgen, Abbott, Novo Nordisk, Novartis, Lonza, .

Biotechnologymarket report provides a detailed analysis of global market size, regional and country-level market size, segmentation market growth, market share, competitive Landscape, sales analysis, the impact of domestic and global market players, value chain optimization, trade regulations, recent developments, opportunities analysis, strategic market growth analysis, product launches, area marketplace expanding, and technological innovations.

Market Segmentations: Global Biotechnology market competition by top manufacturers, with production, price, revenue (value) and market share for each manufacturer.

Based on type, report split into DNA Sequencing, Nanobiotechnology, Tissue engineering and Regeneration, Fermentation, Cell Based Assay, PCR Technology, Chromatography Market, Others.

Based on the end users/applications, this report focuses on the status and outlook for major applications/end users, consumption (sales), market share and growth rate for each application, including Health, Food & Agriculture, Natural Resources & Environment, Industrial Processing, Bioinformatics.

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The report introduces Biotechnology basic information including definition, classification, application, industry chain structure, industry overview, policy analysis, and news analysis. Insightful predictions for the Biotechnology Market for the coming few years have also been included in the report.

In the end, Biotechnologyreport provides details of competitive developments such as expansions, agreements, new product launches, and acquisitions in the market for forecasting, regional demand, and supply factor, investment, market dynamics including technical scenario, consumer behavior, and end-use industry trends and dynamics, capacity, spending were taken into consideration.

Important Key questions answered in Biotechnologymarket report:

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Is Cara Therapeutics Inc (CARA) a Winner in the Biotechnology Industry? – InvestorsObserver

Thursday, June 4th, 2020

The 60 rating InvestorsObserver gives to Cara Therapeutics Inc (CARA) stock puts it near the middle of the Biotechnology industry. In addition to scoring higher than 52 percent of stocks in the Biotechnology industry, CARAs 60 overall rating means the stock scores better than 60 percent of all stocks.

Analyzing stocks can be hard. There are tons of numbers and ratios, and it can be hard to remember what they all mean and what counts as good for a given value. InvestorsObserver ranks stocks on eight different metrics. We percentile rank most of our scores to make it easy for investors to understand. A score of 60 means the stock is more attractive than 60 percent of stocks.

These rankings allows you to easily compare stocks and view what the strengths and weaknesses are of a given company. This lets you find the stocks with the best short and long term growth prospects in a matter of seconds. The combined score incorporates technical and fundamental analysis in order to give a comprehensive overview of a stocks performance. Investors who then want to focus on analysts rankings or valuations are able to see the separate scores for each section.

Cara Therapeutics Inc (CARA) stock is trading at $15.57 as of 3:36 PM on Thursday, Jun 4, a loss of -$0.50, or -3.11% from the previous closing price of $16.07. The stock has traded between $15.57 and $16.25 so far today. Volume today is low. So far 360,678 shares have traded compared to average volume of 569,619 shares.

To screen for more stocks like CARA click here.

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Pharmaceutical & Biotechnology Environmental Monitoring Market 2020 Industry Analysis, Size, Share, Trends, Market Demand, Growth, Opportunities…

Thursday, June 4th, 2020

The market research report published by QYResearch is a brilliant, complete, and much-needed resource for companies, stakeholders, and investors interested in the global Pharmaceutical & Biotechnology Environmental Monitoring market. It informs readers about key trends and opportunities in the global Pharmaceutical & Biotechnology Environmental Monitoring market along with critical market dynamics expected to impact the global market growth. It offers a range of market analysis studies, including production and consumption, sales, industry value chain, competitive landscape, regional growth, and price. On the whole, it comes out as an intelligent resource that companies can use to gain a competitive advantage in the global Pharmaceutical & Biotechnology Environmental Monitoring market.

Key companies operating in the global Pharmaceutical & Biotechnology Environmental Monitoring market include , Danaher Corporation, Thermo Fisher Scientific, Merck KGaA, Eurofins Sinensis, Lonza, Biomerieux, VAI, Cosasco, RMONI, Amphenol Advanced Sensors, Vaisala Pharmaceutical & Biotechnology Environmental Monitoring

Get PDF Sample Copy of the Report to understand the structure of the complete report: (Including Full TOC, List of Tables & Figures, Chart) :

https://www.qyresearch.com/sample-form/form/1436318/global-pharmaceutical-amp-biotechnology-environmental-monitoring-market

Segmental Analysis

Both developed and emerging regions are deeply studied by the authors of the report. The regional analysis section of the report offers a comprehensive analysis of the global Pharmaceutical & Biotechnology Environmental Monitoring market on the basis of region. Each region is exhaustively researched about so that players can use the analysis to tap into unexplored markets and plan powerful strategies to gain a foothold in lucrative markets.

Global Pharmaceutical & Biotechnology Environmental Monitoring Market Segment By Type:

, Monitoring Equipment, Media, Software, Microbiology Services Pharmaceutical & Biotechnology Environmental Monitoring

Global Pharmaceutical & Biotechnology Environmental Monitoring Market Segment By Application:

, Pharmaceutical Industry, Biotechnology Industry, Academic & Research Institutes

Competitive Landscape

Competitor analysis is one of the best sections of the report that compares the progress of leading players based on crucial parameters, including market share, new developments, global reach, local competition, price, and production. From the nature of competition to future changes in the vendor landscape, the report provides in-depth analysis of the competition in the global Pharmaceutical & Biotechnology Environmental Monitoring market.

Key companies operating in the global Pharmaceutical & Biotechnology Environmental Monitoring market include , Danaher Corporation, Thermo Fisher Scientific, Merck KGaA, Eurofins Sinensis, Lonza, Biomerieux, VAI, Cosasco, RMONI, Amphenol Advanced Sensors, Vaisala Pharmaceutical & Biotechnology Environmental Monitoring

Key questions answered in the report:

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TOC

1 Report Overview1.1 Study Scope1.2 Key Market Segments1.3 Players Covered: Ranking by Pharmaceutical & Biotechnology Environmental Monitoring Revenue1.4 Market Analysis by Type 1.4.1 Global Pharmaceutical & Biotechnology Environmental Monitoring Market Size Growth Rate by Type: 2020 VS 2026 1.4.2 Monitoring Equipment 1.4.3 Media 1.4.4 Software 1.4.5 Microbiology Services1.5 Market by Application 1.5.1 Global Pharmaceutical & Biotechnology Environmental Monitoring Market Share by Application: 2020 VS 2026 1.5.2 Pharmaceutical Industry 1.5.3 Biotechnology Industry 1.5.4 Academic & Research Institutes1.6 Coronavirus Disease 2019 (Covid-19): Pharmaceutical & Biotechnology Environmental Monitoring Industry Impact 1.6.1 How the Covid-19 is Affecting the Pharmaceutical & Biotechnology Environmental Monitoring Industry 1.6.1.1 Pharmaceutical & Biotechnology Environmental Monitoring Business Impact Assessment Covid-19 1.6.1.2 Supply Chain Challenges 1.6.1.3 COVID-19s Impact On Crude Oil and Refined Products 1.6.2 Market Trends and Pharmaceutical & Biotechnology Environmental Monitoring Potential Opportunities in the COVID-19 Landscape 1.6.3 Measures / Proposal against Covid-19 1.6.3.1 Government Measures to Combat Covid-19 Impact 1.6.3.2 Proposal for Pharmaceutical & Biotechnology Environmental Monitoring Players to Combat Covid-19 Impact1.7 Study Objectives1.8 Years Considered 2 Global Growth Trends by Regions2.1 Pharmaceutical & Biotechnology Environmental Monitoring Market Perspective (2015-2026)2.2 Pharmaceutical & Biotechnology Environmental Monitoring Growth Trends by Regions 2.2.1 Pharmaceutical & Biotechnology Environmental Monitoring Market Size by Regions: 2015 VS 2020 VS 2026 2.2.2 Pharmaceutical & Biotechnology Environmental Monitoring Historic Market Share by Regions (2015-2020) 2.2.3 Pharmaceutical & Biotechnology Environmental Monitoring Forecasted Market Size by Regions (2021-2026)2.3 Industry Trends and Growth Strategy 2.3.1 Market Top Trends 2.3.2 Market Drivers 2.3.3 Market Challenges 2.3.4 Porters Five Forces Analysis 2.3.5 Pharmaceutical & Biotechnology Environmental Monitoring Market Growth Strategy 2.3.6 Primary Interviews with Key Pharmaceutical & Biotechnology Environmental Monitoring Players (Opinion Leaders) 3 Competition Landscape by Key Players3.1 Global Top Pharmaceutical & Biotechnology Environmental Monitoring Players by Market Size 3.1.1 Global Top Pharmaceutical & Biotechnology Environmental Monitoring Players by Revenue (2015-2020) 3.1.2 Global Pharmaceutical & Biotechnology Environmental Monitoring Revenue Market Share by Players (2015-2020) 3.1.3 Global Pharmaceutical & Biotechnology Environmental Monitoring Market Share by Company Type (Tier 1, Tier 2 and Tier 3)3.2 Global Pharmaceutical & Biotechnology Environmental Monitoring Market Concentration Ratio 3.2.1 Global Pharmaceutical & Biotechnology Environmental Monitoring Market Concentration Ratio (CR5 and HHI) 3.2.2 Global Top 10 and Top 5 Companies by Pharmaceutical & Biotechnology Environmental Monitoring Revenue in 20193.3 Pharmaceutical & Biotechnology Environmental Monitoring Key Players Head office and Area Served3.4 Key Players Pharmaceutical & Biotechnology Environmental Monitoring Product Solution and Service3.5 Date of Enter into Pharmaceutical & Biotechnology Environmental Monitoring Market3.6 Mergers & Acquisitions, Expansion Plans 4 Breakdown Data by Type (2015-2026)4.1 Global Pharmaceutical & Biotechnology Environmental Monitoring Historic Market Size by Type (2015-2020)4.2 Global Pharmaceutical & Biotechnology Environmental Monitoring Forecasted Market Size by Type (2021-2026) 5 Pharmaceutical & Biotechnology Environmental Monitoring Breakdown Data by Application (2015-2026)5.1 Global Pharmaceutical & Biotechnology Environmental Monitoring Market Size by Application (2015-2020)5.2 Global Pharmaceutical & Biotechnology Environmental Monitoring Forecasted Market Size by Application (2021-2026) 6 North America6.1 North America Pharmaceutical & Biotechnology Environmental Monitoring Market Size (2015-2020)6.2 Pharmaceutical & Biotechnology Environmental Monitoring Key Players in North America (2019-2020)6.3 North America Pharmaceutical & Biotechnology Environmental Monitoring Market Size by Type (2015-2020)6.4 North America Pharmaceutical & Biotechnology Environmental Monitoring Market Size by Application (2015-2020) 7 Europe7.1 Europe Pharmaceutical & Biotechnology Environmental Monitoring Market Size (2015-2020)7.2 Pharmaceutical & Biotechnology Environmental Monitoring Key Players in Europe (2019-2020)7.3 Europe Pharmaceutical & Biotechnology Environmental Monitoring Market Size by Type (2015-2020)7.4 Europe Pharmaceutical & Biotechnology Environmental Monitoring Market Size by Application (2015-2020) 8 China8.1 China Pharmaceutical & Biotechnology Environmental Monitoring Market Size (2015-2020)8.2 Pharmaceutical & Biotechnology Environmental Monitoring Key Players in China (2019-2020)8.3 China Pharmaceutical & Biotechnology Environmental Monitoring Market Size by Type (2015-2020)8.4 China Pharmaceutical & Biotechnology Environmental Monitoring Market Size by Application (2015-2020) 9 Japan9.1 Japan Pharmaceutical & Biotechnology Environmental Monitoring Market Size (2015-2020)9.2 Pharmaceutical & Biotechnology Environmental Monitoring Key Players in Japan (2019-2020)9.3 Japan Pharmaceutical & Biotechnology Environmental Monitoring Market Size by Type (2015-2020)9.4 Japan Pharmaceutical & Biotechnology Environmental Monitoring Market Size by Application (2015-2020) 10 Southeast Asia10.1 Southeast Asia Pharmaceutical & Biotechnology Environmental Monitoring Market Size (2015-2020)10.2 Pharmaceutical & Biotechnology Environmental Monitoring Key Players in Southeast Asia (2019-2020)10.3 Southeast Asia Pharmaceutical & Biotechnology Environmental Monitoring Market Size by Type (2015-2020)10.4 Southeast Asia Pharmaceutical & Biotechnology Environmental Monitoring Market Size by Application (2015-2020) 11 India11.1 India Pharmaceutical & Biotechnology Environmental Monitoring Market Size (2015-2020)11.2 Pharmaceutical & Biotechnology Environmental Monitoring Key Players in India (2019-2020)11.3 India Pharmaceutical & Biotechnology Environmental Monitoring Market Size by Type (2015-2020)11.4 India Pharmaceutical & Biotechnology Environmental Monitoring Market Size by Application (2015-2020) 12 Central & South America12.1 Central & South America Pharmaceutical & Biotechnology Environmental Monitoring Market Size (2015-2020)12.2 Pharmaceutical & Biotechnology Environmental Monitoring Key Players in Central & South America (2019-2020)12.3 Central & South America Pharmaceutical & Biotechnology Environmental Monitoring Market Size by Type (2015-2020)12.4 Central & South America Pharmaceutical & Biotechnology Environmental Monitoring Market Size by Application (2015-2020) 13 Key Players Profiles13.1 Danaher Corporation 13.1.1 Danaher Corporation Company Details 13.1.2 Danaher Corporation Business Overview and Its Total Revenue 13.1.3 Danaher Corporation Pharmaceutical & Biotechnology Environmental Monitoring Introduction 13.1.4 Danaher Corporation Revenue in Pharmaceutical & Biotechnology Environmental Monitoring Business (2015-2020)) 13.1.5 Danaher Corporation Recent Development13.2 Thermo Fisher Scientific 13.2.1 Thermo Fisher Scientific Company Details 13.2.2 Thermo Fisher Scientific Business Overview and Its Total Revenue 13.2.3 Thermo Fisher Scientific Pharmaceutical & Biotechnology Environmental Monitoring Introduction 13.2.4 Thermo Fisher Scientific Revenue in Pharmaceutical & Biotechnology Environmental Monitoring Business (2015-2020) 13.2.5 Thermo Fisher Scientific Recent Development13.3 Merck KGaA 13.3.1 Merck KGaA Company Details 13.3.2 Merck KGaA Business Overview and Its Total Revenue 13.3.3 Merck KGaA Pharmaceutical & Biotechnology Environmental Monitoring Introduction 13.3.4 Merck KGaA Revenue in Pharmaceutical & Biotechnology Environmental Monitoring Business (2015-2020) 13.3.5 Merck KGaA Recent Development13.4 Eurofins Sinensis 13.4.1 Eurofins Sinensis Company Details 13.4.2 Eurofins Sinensis Business Overview and Its Total Revenue 13.4.3 Eurofins Sinensis Pharmaceutical & Biotechnology Environmental Monitoring Introduction 13.4.4 Eurofins Sinensis Revenue in Pharmaceutical & Biotechnology Environmental Monitoring Business (2015-2020) 13.4.5 Eurofins Sinensis Recent Development13.5 Lonza 13.5.1 Lonza Company Details 13.5.2 Lonza Business Overview and Its Total Revenue 13.5.3 Lonza Pharmaceutical & Biotechnology Environmental Monitoring Introduction 13.5.4 Lonza Revenue in Pharmaceutical & Biotechnology Environmental Monitoring Business (2015-2020) 13.5.5 Lonza Recent Development13.6 Biomerieux 13.6.1 Biomerieux Company Details 13.6.2 Biomerieux Business Overview and Its Total Revenue 13.6.3 Biomerieux Pharmaceutical & Biotechnology Environmental Monitoring Introduction 13.6.4 Biomerieux Revenue in Pharmaceutical & Biotechnology Environmental Monitoring Business (2015-2020) 13.6.5 Biomerieux Recent Development13.7 VAI 13.7.1 VAI Company Details 13.7.2 VAI Business Overview and Its Total Revenue 13.7.3 VAI Pharmaceutical & Biotechnology Environmental Monitoring Introduction 13.7.4 VAI Revenue in Pharmaceutical & Biotechnology Environmental Monitoring Business (2015-2020) 13.7.5 VAI Recent Development13.8 Cosasco 13.8.1 Cosasco Company Details 13.8.2 Cosasco Business Overview and Its Total Revenue 13.8.3 Cosasco Pharmaceutical & Biotechnology Environmental Monitoring Introduction 13.8.4 Cosasco Revenue in Pharmaceutical & Biotechnology Environmental Monitoring Business (2015-2020) 13.8.5 Cosasco Recent Development13.9 RMONI 13.9.1 RMONI Company Details 13.9.2 RMONI Business Overview and Its Total Revenue 13.9.3 RMONI Pharmaceutical & Biotechnology Environmental Monitoring Introduction 13.9.4 RMONI Revenue in Pharmaceutical & Biotechnology Environmental Monitoring Business (2015-2020) 13.9.5 RMONI Recent Development13.10 Amphenol Advanced Sensors 13.10.1 Amphenol Advanced Sensors Company Details 13.10.2 Amphenol Advanced Sensors Business Overview and Its Total Revenue 13.10.3 Amphenol Advanced Sensors Pharmaceutical & Biotechnology Environmental Monitoring Introduction 13.10.4 Amphenol Advanced Sensors Revenue in Pharmaceutical & Biotechnology Environmental Monitoring Business (2015-2020) 13.10.5 Amphenol Advanced Sensors Recent Development13.11 Vaisala 10.11.1 Vaisala Company Details 10.11.2 Vaisala Business Overview and Its Total Revenue 10.11.3 Vaisala Pharmaceutical & Biotechnology Environmental Monitoring Introduction 10.11.4 Vaisala Revenue in Pharmaceutical & Biotechnology Environmental Monitoring Business (2015-2020) 10.11.5 Vaisala Recent Development 14 Analysts Viewpoints/Conclusions 15 Appendix15.1 Research Methodology 15.1.1 Methodology/Research Approach 15.1.2 Data Source15.2 Disclaimer15.3 Author Details

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Impact of Covid-19 on Agricultural Biotechnology Market Outlook, Revenue, Trends and Forecasts Research Report 2020-2028 – Azizsalon News

Sunday, May 31st, 2020

Agricultural Biotechnology Market is analyzed with industry experts in mind to maximize return on investment by providing clear information needed for informed business decisions. This research will help both established and new entrants to identify and analyze market needs, market size and competition. It explains the supply and demand situation, the competitive scenario, and the challenges for market growth, market opportunities and the threats faced by key players.

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A 360 degree outline of the competitive scenario of the Global Agricultural BiotechnologyMarket is presented by QuinceMarketInsights. It has a massive data allied to the recent product and technological developments in the markets.

It has a wide-ranging analysis of the impact of these advancements on the markets future growth, wide-ranging analysis of these extensions on the markets future growth. The research report studies the market in a detailed manner by explaining the key facets of the market that are foreseeable to have a countable stimulus on its developing extrapolations over the forecast period.

Key players: KWS SAAT SE & Co. KGaA, ChemChina, Limagrain, Nufarm, Marrone Bio Innovations, Performance Plants Inc., Corteva, ADAMA Ltd, MITSUI & CO., LTD, Evogene Ltd., Valent BioSciences LLC, and Bayer AG.

Reasons for buying this report:

By Application (Vaccine, Flower Culturing, Biofuels)

By Organism (Plants, Animals, Microbes)

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A detailed outline of the Global Agricultural BiotechnologyMarket includes a comprehensive analysis of different verticals of businesses. North America, Europe, Asia Pacific, Middle East & Africa, and South America have been considered for the studies on the basis of several terminologies.

This is anticipated to drive the Global Agricultural BiotechnologyMarket over the forecast period. This research report covers the market landscape and its progress prospects in the near future. After studying key companies, the report focuses on the new entrants contributing to the growth of the market. Most companies in the Global Agricultural BiotechnologyMarket are currently adopting new technological trends in the market.

Finally, the researchers throw light on different ways to discover the strengths, weaknesses, opportunities, and threats affecting the growth of the Global Agricultural BiotechnologyMarket. The feasibility of the new report is also measured in this research report.

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Impact of Covid-19 on Agricultural Biotechnology Market Outlook, Revenue, Trends and Forecasts Research Report 2020-2028 - Azizsalon News

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UNITY Biotechnology to Participate in the Goldman Sachs 41st Annual Global Healthcare Conference – GlobeNewswire

Sunday, May 31st, 2020

SAN FRANCISCO, May 28, 2020 (GLOBE NEWSWIRE) -- UNITY Biotechnology (UNITY) [NASDAQ:UBX], a biotechnology company developing therapeutics to extend healthspan by slowing, halting or reversing diseases of aging, today announced that members of its senior management team will participate in the upcoming Goldman Sachs 41st Annual Global Healthcare Conference.

Goldman Sachs 41st Annual Global Healthcare Conference

Date: June 11, 2020Fireside Chat Time: 3:50 PM E.T. Location: Virtual

A live audio webcast of the fireside chat will be available through the Investors & Media section of UNITYs website. An archived replay will be available for 90 days following the event.

About UNITYUNITY is developing therapeutics to extend healthspan with an initial focus on cellular senescence. UNITY believes that the accumulation of senescent cells is a fundamental mechanism of aging and a driver of many common age-related diseases. Cellular senescence is a natural biological state in which a cell permanently halts division. As senescent cells accumulate with age, they begin secreting inflammatory factors, proteases, fibrotic factors, and growth factors, that disturb the tissue micro-environment. This collection of secreted proteins is referred to as the Senescence Associated Secretory Phenotype, or SASP. UNITY is developing senolytic medicines to eliminate senescent cells and thereby stop the production of the SASP, which UNITY believes addresses a root cause of age-related diseases. By stopping the production of the SASP at it source, UNITY believes senolytic medicines could slow, halt, or reverse diseases such as osteoarthritis and age-related eye diseases. More information is available atwww.unitybiotechnology.comor follow us onTwitter.

Investors Endurance AdvisorsMike Zanonimzanoni@enduranceadvisors.com

Media Canale CommunicationsJason Sparkjason@canalecomm.com

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UNITY Biotechnology to Participate in the Goldman Sachs 41st Annual Global Healthcare Conference - GlobeNewswire

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Food Biotechnology Market Overview By Growing Demands, Trends And Business Opportunities 2020 To 2027 – Cole of Duty

Sunday, May 31st, 2020

Trusted Business Insights answers what are the scenarios for growth and recovery and whether there will be any lasting structural impact from the unfolding crisis for the Food Biotechnology market.

Trusted Business Insights presents an updated and Latest Study on Food Biotechnology Market 2019-2026. The report contains market predictions related to market size, revenue, production, CAGR, Consumption, gross margin, price, and other substantial factors. While emphasizing the key driving and restraining forces for this market, the report also offers a complete study of the future trends and developments of the market.The report further elaborates on the micro and macroeconomic aspects including the socio-political landscape that is anticipated to shape the demand of the Food Biotechnology market during the forecast period (2019-2029).It also examines the role of the leading market players involved in the industry including their corporate overview, financial summary, and SWOT analysis.

Get Sample Copy of this Report @ Food Biotechnology Market Research Report Forecast to 2029 (Includes Business Impact of COVID-19)

Abstract, Snapshot, Market Analysis & Market Definition: Food Biotechnology MarketIndustry / Sector Trends

Global Food Biotechnology Market size was valued at over USD 23 billion in 2018 and is anticipated to witness over 10% CAGR up to 2025.

Increasing penetration of advanced technologies to develop new products by modifying plants, animals, and microorganisms genes to provide innovative solutions is driving the market growth. Shifting trends towards healthy lifestyles accompanied by a rise in processed food demand has urged the F&B manufacturers to improve the nutritional content in their products, thereby generating new growth opportunities for the biotech-based industry players. Further, there is a requirement to enhance the shelf life and taste of food by the use of encapsulation techniques and other ingredients.

Strong growth in functional food & beverages and dietary supplements industry is resulting in increased competitiveness, thus propelling the food biotechnology market revenue. As per CCI, the global nutraceutical market including functional F&B and dietary supplements is projected to reach USD 241 billion in 2019, observing around 7% CAGR from 2014 to 2019. Factors such as robust expansion of food industry and low-cost biotech services particular in developing countries has escalated the adoption of services.

Stringent government regulations to enhance product quality and transparency are among the foremost aspects attributing to food biotech solutions. Also, modifications in labeling regulations asking for a declaration of GMOs, allergens, and nutritional content is surging the industry share. Further, consumer-driven movements such as clean label has urged food manufacturers to improve the quality by using natural ingredients instead of artificial constituents.

Changes in climatic conditions over the years has resulted in increased production of genetically modified (GM) crops or ingredients through the use of biotech services. This provides plants with improved resistance to diseases, insecticides, and herbicides, as well as extending the shelf life of the produce. However, growth in the organic food industry can hamper the demand for GM crops, thus affecting the food biotechnology industry share.

Market Segmentation, Outlook & Regional Insights: Food Biotechnology Market

Food Biotechnology Market, By Type

Transgenic segment dominates the global market accounting for over 75% share in 2018. Increasing demand for genetically modified crops to enhance productivity in low producing or harsh climatic conditions will drive segment growth. According to ISAAA, the global utilized area for biotech crops increased from 148 million hectares in 2010 to 190 million hectares in 2017. Countries including the U.S., Brazil, Argentina, Canada, and India holds over 90% of the total area under GM crop cultivation. Farmers shifting from conventional seeds to bio-seeds to improve their profit margins will escalate the market growth.

Germany Food Biotechnology Market Size, By Type, 2018 (USD Million)

Food Biotechnology Market, By Application

Global food biotechnology market through animal segment holds over 34% share in 2018. Increasing necessity to enhance milk production in dairy cattle with growing demand will propel industry expansion. Robust growth in meat consumption such as processed meat accompanied by increasing consumer awareness on nutritional benefits will drive the biotech applications. As per FAO, global meat production is projected to increase, reach around 48MT by 2025. Further, testing services for developing products to suit the human dietary requirements will drive market development.

Global food biotechnology market through plants is projected to account for over USD 22 billion in 2025. The key growth factors include an increase in the development of GM crops with pesticide resistance and abiotic stress tolerance to increase the yield. Reduction in the arable land area will further shift the preference towards biotechnological products. Enhanced focus on innovation of new food ingredients will surge the business revenues. Strong application outlook of biotech solutions to produce high-quality crops and reduce the health risk will augment business expansion.

Food Biotechnology Market, By Region

North America market is anticipated to cross USD 12 billion by 2025. High investments on technological advancements coupled with high consumer spending on nutritious products will augment the industry share. The U.S. is the largest producer of genetically modified crops with 75 million hectares area for biotech crops. Further, the presence of large multinational corporations, increasing private and government R&D investments, supported by favourable government policies will fuel the market growth. Further, positive application outlook of genetically modified yeast in developing new alcoholic beverages will support regional growth.

Asia Pacific Food Biotechnology Market, By Country, 2018 & 2025, (USD Million)

Asia Pacific food biotechnology market is projected to witness over 11% CAGR from 2019 to 2025. Countries including China, India, and Japan together dominate the regional market share. The demand for dietary supplements is increasing due to a shifting trend towards healthy lifestyles, thus increasing the demand for nutritional ingredients. Also, product innovations supported by the rise in per capita income will drive the biotech solutions on health foods. Further, the necessity to augment the agricultural output owing to the rise in population, along with severe climatic variations will drive the biotechnology industry share.

Key Players, Recent Developments & Sector Viewpoints: Food Biotechnology Market

Global market is competitive due to the presence of large multinationals and regional players. Key industry participants in market include BASF SE, Bayer CropScience AG, AquaBounty Technologies, ABS Global, Dow AgroSciences LLC, Arcadia Biosciences, Camson Bio Technologies Ltd, BDF Ingredients Zuchem, and Monsanto. Product development, geographic expansion, mergers, acquisitions, and collaborations are among the key strategies observed in the industry. For instance, in 2017, Bayer and Ginkgo Bioworks announced to launch a company to developing new technologies for engineering the plant microbiome.

Industry Viewpoint

Food biotechnology market is driven by the requirement for improving the productivity and quality of the edible items by altering genes. Growth in the food & beverages industry, increasing population, rising disposable incomes, and health awareness are among the major factors creating a long-term positive impact. Biotechnological product innovations among food manufacturers will provide lucrative opportunities for business growth. North America and Europe are among the early adopters of biotech services, however developing regions are also expected to implement advanced solutions in food industry. The penetration rate is high in Asia Pacific owing to strong R&D investments and the necessity for increasing the food productivity and animal milk output

Key Insights Covered: Exhaustive Food Biotechnology Market1. Market size (sales, revenue and growth rate) of Food Biotechnology industry.2. Global major manufacturers operating situation (sales, revenue, growth rate and gross margin) of Food Biotechnology industry.3. SWOT analysis, New Project Investment Feasibility Analysis, Upstream raw materials and manufacturing equipment & Industry chain analysis of Food Biotechnology industry.4. Market size (sales, revenue) forecast by regions and countries from 2019 to 2025 of Food Biotechnology industry.

Research Methodology: Food Biotechnology Market

Quick Read Table of Contents of this Report @ Food Biotechnology Market Research Report Forecast to 2029 (Includes Business Impact of COVID-19)

Trusted Business InsightsShelly ArnoldMedia & Marketing ExecutiveEmail Me For Any ClarificationsConnect on LinkedInClick to follow Trusted Business Insights LinkedIn for Market Data and Updates.US: +1 646 568 9797UK: +44 330 808 0580

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Impact of Covid-19 Outbreak on Nanoparticles in Biotechnology and Pharmaceuticals Market 2020 Trends, Growth Opportunities, Demand, Application, Top…

Sunday, May 31st, 2020

A report, added to the extensive database of verified Market Research titled Nanoparticles in Biotechnology and Pharmaceuticals Market 2020 by Manufacturer, Region, Type and Application, Forecast up to 2026, is intended to highlight first-hand documentation of all the best implementations in the industry. The report contains an in-depth analysis of current and future market trends, segmentation, industrial opportunities and the future market scenario, taking into account the forecast years 2020 to 2026. It contains extremely important details on the key players in the Nanoparticles in Biotechnology and Pharmaceuticals market as well as growth-oriented practices, that they normally use. The report examines a number of growth drivers and limiting factors. The key forecast information by region, type and application with sales and revenue from 2020 to 2026 is included in this report.

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Top 10 Companies in the Nanoparticles in Biotechnology and Pharmaceuticals Market Research Report:

Competitive landscape:

The report examines the major players, including the profiles of the major players in the market with a significant global and / or regional presence, combined with their information such as related companies, downstream buyers, upstream suppliers, market position, historical background and top competitors based on the Sales with sales contact information.

Regional Description:

The Nanoparticles in Biotechnology and Pharmaceuticals market was analyzed and a proper survey of the market was carried out based on all regions of the world. The regions listed in the report include: North America (United States, Canada, and Mexico), Europe (Germany, France, United Kingdom, Russia, and Italy), Asia-Pacific (China, Japan, Korea, India, and Southeast Asia), South America (Brazil, Argentina , Colombia etc.), Middle East and Africa (Saudi Arabia, United Arab Emirates, Egypt, Nigeria and South Africa). All these regions have been studied in detail and the prevailing trends and different possibilities are also mentioned in the market report.

Sales and sales broken down by application:

Sales and sales divided by type:

In addition, the report categorizes product type and end uses as dynamic market segments that directly impact the growth potential and roadmap of the target market. The report highlights the core developments that are common to all regional hubs and their subsequent impact on the holistic growth path of the Nanoparticles in Biotechnology and Pharmaceuticals market worldwide. Other valuable aspects of the report are the market development history, various marketing channels, supplier analysis, potential buyers and the analysis of the markets industrial chain.

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Table of Content

1 Introduction of Nanoparticles in Biotechnology and Pharmaceuticals Market

1.1 Overview of the Market1.2 Scope of Report1.3 Assumptions

2 Executive Summary

3 Research Methodology of Verified Market Research

3.1 Data Mining3.2 Validation3.3 Primary Interviews3.4 List of Data Sources

4 Nanoparticles in Biotechnology and Pharmaceuticals Market Outlook

4.1 Overview4.2 Market Dynamics4.2.1 Drivers4.2.2 Restraints4.2.3 Opportunities4.3 Porters Five Force Model4.4 Value Chain Analysis

5 Nanoparticles in Biotechnology and Pharmaceuticals Market, By Deployment Model

5.1 Overview

6 Nanoparticles in Biotechnology and Pharmaceuticals Market, By Solution

6.1 Overview

7 Nanoparticles in Biotechnology and Pharmaceuticals Market, By Vertical

7.1 Overview

8 Nanoparticles in Biotechnology and Pharmaceuticals Market, By Geography

8.1 Overview8.2 North America8.2.1 U.S.8.2.2 Canada8.2.3 Mexico8.3 Europe8.3.1 Germany8.3.2 U.K.8.3.3 France8.3.4 Rest of Europe8.4 Asia Pacific8.4.1 China8.4.2 Japan8.4.3 India8.4.4 Rest of Asia Pacific8.5 Rest of the World8.5.1 Latin America8.5.2 Middle East

9 Nanoparticles in Biotechnology and Pharmaceuticals Market Competitive Landscape

9.1 Overview9.2 Company Market Ranking9.3 Key Development Strategies

10 Company Profiles

10.1.1 Overview10.1.2 Financial Performance10.1.3 Product Outlook10.1.4 Key Developments

11 Appendix

11.1 Related Research

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About us:

Verified Market Research is a leading Global Research and Consulting firm servicing over 5000+ customers. Verified Market Research provides advanced analytical research solutions while offering information enriched research studies. We offer insight into strategic and growth analyses, Data necessary to achieve corporate goals and critical revenue decisions.

Our 250 Analysts and SMEs offer a high level of expertise in data collection and governance use industrial techniques to collect and analyse data on more than 15,000 high impact and niche markets. Our analysts are trained to combine modern data collection techniques, superior research methodology, expertise and years of collective experience to produce informative and accurate research.

We study 14+ categories from Semiconductor & Electronics, Chemicals, Advanced Materials, Aerospace & Defence, Energy & Power, Healthcare, Pharmaceuticals, Automotive & Transportation, Information & Communication Technology, Software & Services, Information Security, Mining, Minerals & Metals, Building & construction, Agriculture industry and Medical Devices from over 100 countries.

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Impact of Covid-19 Outbreak on Nanoparticles in Biotechnology and Pharmaceuticals Market 2020 Trends, Growth Opportunities, Demand, Application, Top...

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A Rapid Response Regulatory enabling mechanism facilitated by Department of Biotechnology for COVID 19 – India Education Diary

Sunday, May 31st, 2020

New Delhi: The Department of Biotechnology has taken several proactive measures to streamline the biosafety regulation and to facilitate researchers and industries which are undertaking research and development in Recombinant DNA Technology and Hazardous Microorganisms.

1. Operationalization of Indian Biosafety Knowledge Portal. The Indian Knowledge Biosafety Portal launched in May, 2019 was made fully operationalized and now the Department is receiving all new applications through online portal only. This has made the whole process transparent and time bound.

2. Notification of Revised Simplified Guidelines on Import, Export and Exchange of GE Organisms and Product Thereof for R&D Purpose: The Department issued the Revised Guidelines in January, 2020 in which Institutional Biosafety Committee have been delegated authority to take decisions on applications of import export and exchange of GE organisms and product thereof for R&D purpose for RG1 and RG2 items.

3. Facilitation of Research and Development on COVID-19: Considering the emerging situations of spread of Coronavirus and with the understanding on requirement of rapid research and development for COVI-19, the Department has proactively taken several steps to facilitate researchers and industries involved in research on COVID19. DBT has issued following guidelines, orders and checklist on COVID 19:

Rapid Response Regulatory Framework for COVID-19 to deal with application for development of vaccines, diagnostics, prophylactics and therapeutics has been notified on 20.03.2020DBT notified Interim Guidance Document on Laboratory Biosafety to Handle COVID-19 Specimens on 08.04.2020.IBSCs are allowed to conduct their meeting through video conferencing up to 30thJune, 2020.Rapid response regulatory framework for development of recombinant DNA COVID 19 vaccine was issued on 26.05.2020.

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A Rapid Response Regulatory enabling mechanism facilitated by Department of Biotechnology for COVID 19 - India Education Diary

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COVID-19: Responding to the business impacts of Pharmaceutical & Biotechnology Environmental Monitoring Market Trends and Segments 2019-2027 …

Sunday, May 31st, 2020

A recent market study on the global Pharmaceutical & Biotechnology Environmental Monitoring market reveals that the global Pharmaceutical & Biotechnology Environmental Monitoring market is expected to reach a value of ~US$ XX by the end of 2029 growing at a CAGR of ~XX% during the forecast period (2019-2029).

The Pharmaceutical & Biotechnology Environmental Monitoring market study includes a thorough analysis of the overall competitive landscape and the company profiles of leading market players involved in the global Pharmaceutical & Biotechnology Environmental Monitoring market. Further, the presented study offers accurate insights pertaining to the different segments of the global Pharmaceutical & Biotechnology Environmental Monitoring market such as the market share, value, revenue, and how each segment is expected to fair post the COVID-19 pandemic.

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The following doubts are addressed in the market report:

Key Highlights of the Pharmaceutical & Biotechnology Environmental Monitoring Market Report

The presented report segregates the Pharmaceutical & Biotechnology Environmental Monitoring market into different segments to ensure the readers gain a complete understanding of the different aspects of the Pharmaceutical & Biotechnology Environmental Monitoring market.

Do You Have Any Query Or Specific Requirement? Ask to Our Industry [emailprotected] https://www.marketresearchhub.com/enquiry.php?type=E&repid=2641259&source=atm

Segmentation of the Pharmaceutical & Biotechnology Environmental Monitoring market

Competitive Outlook

This section of the report throws light on the recent mergers, collaborations, partnerships, and research and development activities within the Pharmaceutical & Biotechnology Environmental Monitoring market on a global scale. Further, a detailed assessment of the pricing, marketing, and product development strategies adopted by leading market players is included in the Pharmaceutical & Biotechnology Environmental Monitoring market report.

Competition AnalysisIn the competitive analysis section of the report, leading as well as prominent players of the global Pharmaceutical & Biotechnology Environmental Monitoring market are broadly studied on the basis of key factors. The report offers comprehensive analysis and accurate statistics on revenue by the player for the period 2015-2020. It also offers detailed analysis supported by reliable statistics on price and revenue (global level) by player for the period 2015-2020.On the whole, the report proves to be an effective tool that players can use to gain a competitive edge over their competitors and ensure lasting success in the global Pharmaceutical & Biotechnology Environmental Monitoring market. All of the findings, data, and information provided in the report are validated and revalidated with the help of trustworthy sources. The analysts who have authored the report took a unique and industry-best research and analysis approach for an in-depth study of the global Pharmaceutical & Biotechnology Environmental Monitoring market.The following players are covered in this report:Danaher CorporationThermo Fisher ScientificMerck KGaAEurofins SinensisLonzaBiomerieuxVAICosascoRMONIAmphenol Advanced SensorsVaisalaPharmaceutical & Biotechnology Environmental Monitoring Breakdown Data by TypeMonitoring EquipmentMediaSoftwareMicrobiology ServicesPharmaceutical & Biotechnology Environmental Monitoring Breakdown Data by ApplicationPharmaceutical IndustryBiotechnology IndustryAcademic & Research Institutes

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Facilitating Research and Innovation: Establishment of 4 COVID-19 Bio Banks by the Department of Biotechnology – India Education Diary

Sunday, May 31st, 2020

New Delhi: For the mitigation of COVID-19 pandemic, R&D efforts are directed at the development of vaccines, diagnostics and therapeutics. The specimens collected from COVID-19 positive subjects can be a valuable resource for the R&D efforts. NITI Aayog has recently issued guidelines for sharing of bio specimens and data for research related to COVID-19. As per the directives of the Cabinet Secretary, the Indian Council of Medical Research (ICMR) has notified 16 bio-repositories for collecting, storing and maintaining clinical samples (oropharyngeal/ nasopharyngeal swabs, broncheoalveolar lavage, sputum, blood, urine and stool) of COVID-19 patients.

The enlistment of 16 Bio Repositories are as follows: ICMR 9, DBT 4 and CSIR 3. The four Bio Repositories under the purview of the Department of Biotechnology are, NCR-Biotech Science Cluster (i) THSTI, Faridabad Clinical samples (ii) RCB Faridabad Viral samples, Institute of Life Sciences, Bhubaneswar, InStem, Bangalore and ILBS, New Delhi .Oropharyngeal / nasopharyngeal swabs, bronchoalveolar lavage, sputum, blood, urine and stool of COVID19 patients will be collected and archived for future use to develop validated diagnostics, therapeutics, vaccines etc.

These designated facilities will develop uniform Standard Operating Procedures (SoPs) for sample collection, transportation, aliquoting, storage, and sharing. The role of bio-banks for COVID-19 samples would be development of a vaccine and treatments; guidance regarding handling, including nasopharyngeal swabs; and conditions under which the higher BSL-3 practices should be followed for example, when working with cultures of the coronavirus specimens. The Department of Biotechnology would be supporting these COVID-19 designated Bio-bank facilities through a well strategized future plan so that novel technological interventions can be developed in due course of time. These designated bio repositories will use the clinical samples for R&D purpose in their respective Institutes.

In addition, they are also authorized to share the samples with academia, industry and commercial entities involved in development of diagnostics, therapeutics, vaccines etc., after scrutinising the purpose of the request and ensuring benefit to the country. Sharing of Biospecimens both Clinical and Viral is going to be key for new technology and product development by our researchers, start-ups and industry, a critical step in our journey towards becoming an Atmanirbhar Bharat.

A Rapid Response Regulatory enabling mechanism facilitated by Department of Biotechnology for COVID 19

The Department of Biotechnology has taken several proactive measures to streamline the biosafety regulation and to facilitate researchers and industries which are undertaking research and development in Recombinant DNA Technology and Hazardous Microorganisms.

1. Operationalization of Indian Biosafety Knowledge Portal. The Indian Knowledge Biosafety Portal launched in May, 2019 was made fully operationalized and now the Department is receiving all new applications through online portal only. This has made the whole process transparent and time bound.

2. Notification of Revised Simplified Guidelines on Import, Export and Exchange of GE Organisms and Product Thereof for R&D Purpose: The Department issued the Revised Guidelines in January, 2020 in which Institutional Biosafety Committee have been delegated authority to take decisions on applications of import export and exchange of GE organisms and product thereof for R&D purpose for RG1 and RG2 items.

3. Facilitation of Research and Development on COVID-19: Considering the emerging situations of spread of Coronavirus and with the understanding on requirement of rapid research and development for COVI-19, the Department has proactively taken several steps to facilitate researchers and industries involved in research on COVID19. DBT has issued following guidelines, orders and checklist on COVID 19:

Rapid Response Regulatory Framework for COVID-19 to deal with application for development of vaccines, diagnostics, prophylactics and therapeutics has been notified on 20.03.2020DBT notified Interim Guidance Document on Laboratory Biosafety to Handle COVID-19 Specimens on 08.04.2020.IBSCs are allowed to conduct their meeting through video conferencing up to 30thJune, 2020.Rapid response regulatory framework for development of recombinant DNA COVID 19 vaccine was issued on 26.05.2020Scaling up of COVID testing centres (Hub and spoke model) inNationalresearch laboratories and Universities

To scale up testing and enhance the reach across the countryCity /Regional clusters have been established in a Hub and Spoke Model to scale-up testing of COVID-19 samples in government institutions across the country. Institutes and Laboratories which have the capacity and expertise for both sample collection, handling/processing (BSL-2 facility) and testing (RT-PCR) serve as the hubs and they involve a number of laboratories which have RT PCR machines and the requisite manpower as their extended Testing facilities.

The Hubs are Government laboratories approved by respective Ministries /Departments (DBT, DST, CSIR, DAE, DRDO, ICAR etc) as per ICMR guidelines. So far 19 City /Regional clusters have been established in Bangalore, Delhi/NCR, Hyderabad, Thiruvananthapuram, Chandigarh/Mohali, Bhubaneshwar, Nagpur, Pune, Mumbai, Lucknow, Chennai, Kolkata, North Eastern Region, Jammu & Kashmir, Ahmedabad, Madhya Pradesh, Rajasthan, Banaras, Palampur and Delhi city.

About 100 institutions have been involved and over 1,60,000 samples tested. Seven DBT Autonomous institutes have been approved as hubs by ICMR and they are performing testing for diagnosis of COVID-19 (RGCB, THSTI, ILS, inStem, NCCS, CDFD, NIBMG).

They are also functioning as hubs in the respective Cities/Regions and coordinating the efforts with a number of other premier Central and State Government institutions. In addition, they are working closely with the respective State Governments in obtaining samples for testing and are reporting every day to ICMR on their testing results. Collectively in about 4 weeks, these clusters have done nearly 1,70,000 tests. These clusters will now be scaled to nearly 50 in next 4 weeks and reach remote corners of the country.

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Nautilus Biotechnology Raises $76 Million in Series B Funding to Be the First to Quantify the Human Proteome – Yahoo Finance

Wednesday, May 27th, 2020

Vulcan Capital-led investment will enable Nautilus to bring a next-generation, single-molecule proteomics platform to market

Nautilus Biotechnology, a company pioneering a high-throughput, low-cost platform for analyzing and quantifying the human proteome, today announced it has raised $76 million in an oversubscribed Series B offering that closed on Monday, May 18, 2020. Nautilus total funding now exceeds $100 million. The Nautilus platform will deliver single-molecule sensitivity more quickly, more completely, and less expensively than is possible with existing technologies. This deeper, richer understanding of proteins will enable a dramatic acceleration of basic science research, significantly improve the success rate of therapeutic development, and speed the adoption of personalized and predictive medicine.

This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20200521005020/en/

Nautilus Biotechnology founders Sujal Patel and Parag Mallick (Photo: Business Wire)

The funding round was led by Vulcan Capital, the multi-billion-dollar investment arm of Vulcan Inc., the company founded by Microsoft co-founder and philanthropist Paul G. Allen. In addition to Vulcan, Perceptive Advisors, Bezos Expeditions, and Defy Partners were new investors in the Series B offering. Previous investors AME Cloud Ventures, Andreessen Horowitz, Bolt, and Madrona Venture Group also participated in the round. The capital will be used to accelerate development of Nautilus proprietary proteomics platform and the expansion of scientific and engineering staff across a variety of levels and disciplines.

Nautilus was co-founded in 2016 by Sujal Patel, founder and CEO of Isilon Systems, a publicly-traded company that sold to EMC in 2010 for $2.6B, and Parag Mallick, PhD, Associate Professor of Radiology at Stanford University and a member of BioX, Stanford's pioneering interdisciplinary biosciences institute, and the Canary Center for Cancer Early Detection. The leadership team combines its entrepreneurial and research backgrounds to solve the challenge of more easily and completely quantifying the proteins that drive every aspect of human physiology. That limitation has impeded scientific and pharmaceutical R&D and Nautilus platform will enable a more comprehensive understanding of cellular and organismic biology.

"Existing proteomics technologies are slow, expensive, incomplete, and lack the sensitivity to deliver deep and meaningful insight into biological processes," said Nautilus co-founder and CEO, Sujal Patel. "Bringing together Parags breakthrough science with my deep understanding of large-scale IT has enabled us to approach the problem in a fundamentally new, more holistic way. Our value derives from a unique, interdisciplinary combination of biochemistry, computer science, and substantial business experience."

"The potential of proteomics has not been fully realized because of the limitations of current analysis methods," said Lee Hartwell, PhD, President and Director Emeritus of the Fred Hutchinson Cancer Research Center, 2001 co-recipient of the Nobel Prize in Physiology and Medicine, and member of Nautilus Scientific Advisory Board. "A greater resolution of the proteome will make it possible for the entire scientific and pharma R&D communities to undertake a wider range of high-value scientific inquiries, thereby accelerating both their research and the benefits that can accrue to human health."

Story continues

"Advancing scientific research and technology is at our core," said Stuart Nagae, Director of Venture Capital at Vulcan Capital. "With over a decade of experience investing in biotech and proteomics innovation, we believe that a reimagining of proteomics is long overdue. Nautilus has put together a special team with the vision, creativity, and experience to achieve that breakthrough, and execute on their vision."

ABOUT NAUTILUS BIOTECHNOLOGY

Based in San Carlos, CA and Seattle, WA, Nautilus is a biotechnology company whose proteomics platform will deliver superior sensitivity far more quickly, more completely, and less expensively than is currently possible. By breaking through the limitations of existing technologies, and effectively democratizing proteomics, Nautilus will enable a dramatic acceleration of basic science research, significantly improve the success rate of therapeutic development, and usher in a new era of personalized and predictive medicine. Find Nautilus online: http://www.nautilus.bio

ABOUT VULCAN CAPITAL

Vulcan Capital is the multi-billion-dollar investment arm of Vulcan Inc., the company founded by Microsoft co-founder and philanthropist Paul G. Allen. Vulcan Capital focuses on generating long-term value appreciation across a portfolio, which spans diverse industry sectors and investment asset classes, ranging from early-stage venture investments to public equity value investing, leveraged buyouts, acquisitions, special situations and fixed income. Vulcan Capital was formed in 2003 and is headquartered in Seattle with additional offices in Palo Alto and Singapore.

View source version on businesswire.com: https://www.businesswire.com/news/home/20200521005020/en/

Contacts

Nautilus Biotechnologypress@nautilus.bio

Kerry WalkerWalker Communicationskerry@walkercomms.com

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CohBar’s CEO to Participate on the New Breakthroughs in Aging Biology Panel at the BIO 2020 Digital Conference – GlobeNewswire

Wednesday, May 27th, 2020

MENLO PARK, Calif., May 27, 2020 (GLOBE NEWSWIRE) -- CohBar, Inc. (NASDAQ: CWBR), a clinical stage biotechnology company developing mitochondria based therapeutics to treat chronic diseases and extend healthy lifespan, today announced its Chief Executive Officer, Steven Engle will be a participant on the panel titled Redefining What it Means to Get Old: New Breakthroughs in Aging Biology at the BIO 2020 Digital Conference, to be held on June 8-12, 2020.

The panel, featuring Nathaniel David, Co-Founder and President of Unity Biotechnology, Tom Hughes, CEO of Navitor Pharmaceuticals and Steven Engle, CEO of CohBar, will be moderated by Hannah Kuchler, US Pharma and Biotech Correspondent for the Financial Times. The panelists are leaders and trail blazers in the field of aging who are pioneering research in cellular senescence, mTORC dysregulation and mitochondrial dysfunction. They will discuss recent scientific breakthroughs which go beyond masking the pain associated with age-related diseases to developing therapies designed to intervene and target the underlying mechanisms of these diseases. This panel session will be available on demand for BIO Digital attendees beginning on June 8, 2020. Also during the conference, Mr. Engle will present a corporate overview on CohBars technology platform, which will be available on demand as well.

BIO is the world's largest trade association representing biotechnology companies, academic institutions, state biotechnology centers and related organizations across the United States and in more than 30 other nations. BIO members are involved in the research and development of innovative healthcare, agricultural, industrial and environmental biotechnology products. BIO also produces the BIO International Convention, the worlds largest gathering of the biotechnology industry, along with industry-leading investor and partnering meetings held around the world.

About CohBar

CohBar (NASDAQ: CWBR) is a clinical stage biotechnology company focused on the research and development of mitochondria based therapeutics, an emerging class of drugs for the treatment of chronic and age-related diseases. Mitochondria based therapeutics originate from the discovery by CohBars founders of a novel group of naturally occurring mitochondrial-derived peptides within the mitochondrial genome that regulate metabolism and cell death, and whose biological activity declines with age. To date, the company has discovered more than 100 mitochondrial derived peptides and generated over 1,000 analogs. CohBars efforts focus on the development of these peptides into therapeutics that offer the potential to address a broad range of diseases, including nonalcoholic steatohepatitis (NASH), obesity, fibrotic diseases, cancer, acute respiratory distress syndrome (ARDS), type 2 diabetes, and cardiovascular and neurodegenerative diseases. The companys lead compound, CB4211, is in the Phase 1b stage of a Phase 1a/1b clinical trial for NASH and obesity. This clinical trial is currently paused due to the COVID-19 pandemic. In addition, CohBar has four preclinical programs, two in cancer, one in fibrotic diseases and one in COVID-19 associated ARDS and type 2 diabetes.

For additional company information, please visit http://www.cohbar.com.

Forward-Looking Statements

This news release contains forward-looking statements which are not historical facts within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements are based only on our current beliefs, expectations and assumptions regarding the future of our business, future plans and strategies, projections, anticipated events and other future conditions. In some cases you can identify these statements by forward-looking words such as believe, may, will, estimate, continue, anticipate, intend, could, should, would, project, plan, expect, goal, seek, future, likely or the negative or plural of these words or similar expressions. Examples of such forward-looking statements include but are not limited to statements regarding anticipated outcomes of research and clinical trials for our mitochondria based therapeutic (MBT) candidates; expectations regarding the growth of MBTs as a significant future class of drug products; and statements regarding anticipated therapeutic properties and potential of our mitochondrial peptide analogs and MBTs. You are cautioned that such statements are not guarantees of future performance and that actual results or developments may differ materially from those set forth in these forward-looking statements. Factors that could cause actual results to differ materially from these forward-looking statements include: our ability to successfully advance drug discovery and development programs, including the delay or termination of ongoing clinical trials; our possible inability to mitigate the prevalence and/or persistence of the injection site reactions, receipt of unfavorable feedback from regulators regarding the safety or tolerability of CB4211 or the possibility of other developments affecting the viability of CB4211 as a clinical candidate or its commercial potential; results that are different from earlier data results including less favorable than and that may not support further clinical development; our ability to raise additional capital when necessary to continue our operations; our ability to recruit and retain key management and scientific personnel; the risk that our intellectual property may not be adequately protected; our ability to establish and maintain partnerships with corporate and industry partners; and risks related to the impact on our business of the COVID-19 pandemic or similar public health crises. Additional assumptions, risks and uncertainties are described in detail in our registration statements, reports and other filings with the Securities and Exchange Commission and applicable Canadian securities regulators, which are available on our website, and at http://www.sec.gov or http://www.sedar.com.

You are cautioned that such statements are not guarantees of future performance and that our actual results may differ materially from those set forth in the forward-looking statements. The forward-looking statements and other information contained in this news release are made as of the date hereof and CohBar does not undertake any obligation to update publicly or revise any forward-looking statements or information, whether as a result of new information, future events or otherwise, unless so required by applicable securities laws. Nothing herein shall constitute an offer to sell or the solicitation of an offer to buy any securities.

Contacts: Jordyn TaraziDirector of Investor RelationsCohBar, Inc.(650) 445-4441Jordyn.tarazi@cohbar.com

Joyce AllaireLifeSci Advisors, LLCjallaire@lifesciadvisors.com

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