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BioPharm International
June 9, 2020
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TOP STORIES


COVID-19 Update

Updates on COVID-19 vaccine candidates, FDA policies, company partnerships, and more.
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Gavi Launches $2-Billion COVID-19 Vaccine Funding Initiative

The Gavi advance market commitment for COVID-19 vaccines is a new financing instrument aimed at incentivizing vaccine manufacturers to produce sufficient and affordable quantities of COVID-19 vaccines.
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Featured Resources from BioPharm International
View our online resource center, sponsored by GE Healthcare, to explore a case study and articles on gaining and retaining skilled labor, modular bioprocessing, the good and bad of biosilimiars, and more.
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Industry News


EC Grants Marketing Authorization for
Subcutaneous Formulation of Daratumumab

The European Commission has granted marketing authorization to the Janssen Pharmaceutical Companies of Johnson & Johnson for Darzalex (daratumumab) subcutaneous formulation to treat adults with multiple myeloma.
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Vaccine “Hesitancy” Threatens COVID
Immunization Efforts

Despite the clear danger of COVID-19 to global health, vaccine opponents have gained ground, as fearful populations lose faith in the capabilities of industry and government to protect public health.
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MORE INDUSTRY NEWS
 
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Innovative Solutions for Protein Analysis and Purification: mAbs and Oligos
An online resource to discover an innovative solution for protein analysis and purification. This site includes useful webcasts, application notes, and more.
Discover now »

 
 
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Biopharma News


Eli Lilly Launches First Human Study of a Potential COVID-19 Antibody Treatment

The medicine is the first outcome of the collaboration between Lilly and AbCellera to create antibody therapies for the prevention and treatment of COVID-19.
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Netherlands Partnership to Develop an Intranasal COVID-19 Vaccine

The new vaccine would be made with a Newcastle disease virus vector that expresses the immunogenic spike protein of SARS-CoV-2
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More Biopharma News
 

Supplier News


CordenPharma Expands Lipid Supply for Moderna

CordenPharma announces expansion of lipid excipients supply for coronavirus vaccine scale up.
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Novavax Contracts to Expand Adjuvant Production

Agreements with the PolyPeptide Group and AGC Biologics will scale up production of the Novavax Matrix-M adjuvant.
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More Supplier News

Regulatory News


Mixed Opinions on Post-Brexit Approach to Northern Ireland Protocol

The protocol on Northern Ireland (NI) once Brexit has been completed has received mixed opinions in industry, according to various press releases.
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Generic Drugs in Spotlight as Pandemic Creates Shortages

FDA and the US Congress support innovation and access to cheaper medicines.
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More Regulatory News

FEATURED TOPICS

UPSTREAM PROCESSING

Single-Use Bioreactors: To Scale Up or Scale Out?

Industry experts debate the pros and cons of “going bigger” than the 2000-L industry norm in a single vessel.
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REGULATORY BEAT

Modern Drug Manufacturing Key to COVID-19 Response

Policy makers seek to ensure supplies of new therapies and to limit shortages.
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PEER-REVIEWED RESEARCH

Comparing Facility Layout Options for Managing Business and Operating Risks

The authors present a risk analysis of the impact of various business and operating risks on three facility layout strategies.
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ANALYTICAL METHODS

Biopharma Analysis Benefits from New
Technology and Methods

Analytical solutions are improving for raw material testing, process development, drug product release, and more.
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PRODUCT/SERVICES PROFILE

Catalent

Catalent Biologics has capabilities and experience in the development, manufacturing, and analytical services for new biological entities, cell and gene therapies, biosimilars, and antibody-drug conjugates.
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WEBCASTS


Validation of an LC-MS Multi-Attribute Method (MAM) Supporting Biopharma Process Characterization
Tuesday, June 30, 2020 at 10am EDT | 9am CDT | 2pm BST | 3pm CEST
Learn More



eBook

Regulatory Sourcebook and Reference, March 2020

The Pharmacopoeia Compliance Series features a description of ways biopharma companies can participate in monograph development, a case study of a practical approach to pharmacopoeial compliance, and a summary of this 12-part series.

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