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BioPharm International
May 26, 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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BARDA Commits $1.2 Billion to AstraZeneca Vaccine Program

Funding from the US government could lead to 300 million coronavirus vaccine doses by October 2020.
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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


NIIMBL Funds Projects with $10 Million for Advances in Biopharma Manufacturing Innovation

This latest round of funding adds 14 new technology projects, workforce development, and Global Health Fund projects to NIIMBL's portfolio.
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International Regulators Work to Coordinate
Pandemic Response

The International Coalition of Medicines Regulatory Authorities held a virtual meeting of regulators from around the world to discuss policy issues and regulatory requirements to respond to the ongoing COVID-19 pandemic.
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KNAUER supports SARS-CoV-2 research
Liquid chromatography is a central tool in research revolving around vaccine and therapeutic development for SARS-CoV-2. Chromatography is not only limited to one aspect of research. It can be used in multiple ways ranging from analytical tasks to preparative purification and protein purification. With more than 55 years’ experience in research, KNAUER is a committed partner to help advance SARS-CoV-2 research.
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Biopharma News


mRNA Vaccine Shows Positive Interim Phase I Results

Participants in two dosing cohorts in Moderna’s mRNA-1273 study reached or exceeded neutralizing antibody titers generally seen in convalescent sera.
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CanSino Biologics, Precision NanoSystems to
Co-develop COVID-19 RNA Vaccine

CanSinoBIO will license-in Precision NanoSystems' proprietary RNA vaccine platform technology while the latter leads the development of the RNA vaccine formulation.
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Supplier News


Vibalogics Manufactures Clinical Trial Material for Janssen COVID-19 Vaccine Candidate

Vibalogics is contracted to manufacture Janssen's COVID-19 candidate vaccine at its GMP-accredited facility in Cuxhaven, Germany.
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Ori Biotech and CellGenix Collaborate on Closed-System, Cell and Gene Therapy Manufacturing

Ori Biotech is partnering with manufacturers and materials suppliers to develop an automated system for cell and gene therapy manufacturing.
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Regulatory News


International Coordination on COVID-19
Treatments Necessary, Says EMA

The European Medicines Agency is emphasizing the need for the research community to pool resources to determine which COVID-19 treatments and preventions are safe and effective.
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EU Member States Meet to Discuss Drug
Shortages During COVID-19

The EU Executive Steering Group on Shortages of Medicines Caused by Major Events met on May 13, 2020 to discuss measures the European Union is taking to ensure the availability of medicines during the COVID-19 pandemic.
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More Regulatory News

FEATURED TOPICS

DOWNSTREAM PROCESSING

Fluid Handling Considerations

Pumps and other components meet the demands of single-use systems in biopharmaceutical downstream processing.
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PEER-REVIEW RESEARCH

Shaping IR Spectroscopy into a Powerful Tool for Biopharma Characterizations

In this peer-reviewed article, the authors present a series of experimental studies showcasing the performance of MMS in secondary-structure biopharma characterization and compare it with conventional FTIR data.
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ANALYTICS

Building Better Bioassays

Next-generation therapeutics and regulatory requirements create demand for complex, fit-for-purpose tests
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MANUFACTURING

Gene Therapies Push Viral Vector Production

Viral vectors show promise as a delivery mechanism for gene therapy, but which virus types are commercially viable?
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WEBCASTS


Viral Vector Process Development: Applying CE and MS Techniques for In-Process Testing
Wednesday, May 27, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST
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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


Accurate Weighing of Reference Standards in a QC Laboratory
Thursday, May 28, 2020 at 11am EDT| 8am PDT| 4pm BST| 5pm 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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