3 Things Manufacturers Need to Know About the New Annex 1 Revision

In August 2023, long-awaited drug manufacturing regulations took effect with the implementation of the European Commission’s...

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Key Considerations When Partnering with a CDMO for Your Plasma-Derived Therapies

Plasma contains an array of beneficial constituents that, when purified and concentrated, can be administered as medicines to...

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4 Steps for a Smooth Tech Transfer When Working with a CDMO

In our recent article with BioPharma Dive, Emergent's Shelly Buhay, Director of MS&T and Dan Perrin, Director of Manufacturing...

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How to Mitigate Risk for Biologics During Fill/Finish Manufacturing

As more biologics move through research and development, the demand for specialized aseptic fill/finish services has steadily...

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The Demand for Nanoparticles in Drug Formulation is Rising

Demand for nanoparticles in the biopharmaceutical industry is on the rise. Production of these tiny particles, which can protect...

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Focus on Fill and Finish

Kelly Christiansen, vice president & general manager of Emergent CDMO's Rockville drug product manufacturing facility recently...

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WANT MORE INFORMATION?

Learn more about Emergent Bioservices' work and the many milestones we’ve reached in our news release archive below.  If you’re a media representative, please feel free to contact us at cdmo@ebsi.com.

Interested in learning more about Emergent BioSolutions, Inc.? Please visit emergentbiosolutions.com.

WANT MORE INFORMATION?

Learn more about Emergent Bioservices work and the many milestones we’ve reached in our news release archive below.  If you’re a media representative, please feel free to contact us at mediarelations@ebsi.com.

Interested in learning more about Emergent BioSolutions, Inc.? Please visit emergentbiosolutions.com.