The FDA daily adverse event dashboard updates are designed to provide faster access to safety information for drugs and biologics. By offering FDA daily adverse event dashboard updates, the agency aims to reduce delays and improve the transparency of reported data. Background on the FAERS System The FDA Adverse Event […]
FOIA’d FDA ‘Establishment Inspection Reports’ of Pfizer COVID Vaccine Manufacturing Facilities Reveal “Inadequate Quality Oversight,” Deficient Deviation Investigations, Ignored Standard Operating Procedures, and More.
Amy Kelly, COO of DailyClout.io and Project Director for the WarRoom/DailyClout Pfizer and Moderna Documents Analysis Project, received a partial production of documents in response to her Freedom of Information Act (FOIA) request submitted to the Food and Drug Administration (FDA) for “all FDA inspection reports from inspections of Pfizer […]