
FDA Unveils Extensive Manufacturing Violations at Emergent
A FDA report cites multiple ongoing violations that undermine assurance of quality in products from this plant and the need for a continuing “pause” in production.
Just in case anyone suspected FDA of over-reacting to problems at this troubled vaccine production site—or that any poor-quality materials could be released—FDA officials have taken the unusual step of issuing the closeout report (Form 483) on its just-completed re-inspection of Emergent BioSolutions’ Baltimore manufacturing facility. The report cites multiple ongoing violations that undermine assurance of quality in products from this plant and the need for a continuing “pause” in production.
FDA Acting Commissioner Janet Woodcock and Peter Marks, director of the Center for Biologics Evaluation and Research (CBER), issued a
FDA inspectors found
The situation now has drawn attention on Capitol Hill. Leaders of the House Oversight & Reform Committee and its Select Subcommittee on the Coronavirus Crisis have
Woodcock and Marks emphasize that they are “doing everything we can” to ensure that COVID-19 vaccines for Americans meet FDA’s high standards for quality, safety, and effectiveness. The result, they hope, is that FDA will maintain the public’s trust in its operations.




