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As Emergent Partnership Dissolves, BARDA Looks To Revamp Post-COVID Pandemic Preparedness

 
• By Bowman Cox

BARDA terminates CIADM contract in wake of vaccine cross-contamination incident, begins discussion with industry about next steps for rapid pandemic response capabilities.

Workers develop vaccines for next pandemic
preparing for the right pandemic partnership • Source: Alamy

An early end to a troubled pandemic preparedness partnership between Emergent BioSolutions, Inc. and the US government’s Biomedical Advanced Research and Development Authority came last week as the agency prepared to turn the page on its COVID-19 pandemic response.

The partnership, one of BARDA’s two centers for innovation in advanced development and manufacturing, or CIADMs, was forged in 2012...

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• By Vibha Ravi

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• By Derrick Gingery

The program would allow early interactions with FDA staff to speed construction and approval of pharmaceutical manufacturing facilities in the US, but will staff be available?

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• By Neena Brizmohun

While titanium dioxide is banned as a food additive in the EU, the European Medicines Agency has convinced the European Commission to allow its continued use in the many thousands of medicines in which it is currently used.

UK Medicines Shortages Inquiry Eyes Full Reshoring of Drug Manufacturing

 
• By Neena Brizmohun

A newly launched UK government inquiry is seeking to learn how viable it would be to bring back domestic control over the entire drug manufacturing pipeline.

More from Compliance

Big PBM Dominance Enabled By Affiliated Third Party Administrators Limiting Choices, FTC Told

 
• By Cathy Kelly

Complaints about TPAs offer an explanation of why self-funded employers continue to use the big three PBMs despite concerns about those relationships. Proposed solutions include banning retaliatory fees and data withholding.

EU 15% Tariff Deal Still Leaves Questions For Pharma On Possible Grace Period, Generic Exemption

 
• By Jessica Merrill

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No Surprise Here: Foreign Drug Facilities Should Expect Surprise Inspections, US FDA Says

 
• By Sue Sutter

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