Judicial Watch has released the 58 pages of records from the U.S. Food and Drug Administration (FDA) showing that a Pfizer study surveyed 23 people in 2021 to gauge reactions to its Covid vaccine booster before asking the FDA to approve it.
The FDA indicated that this production of records “represents our complete response to your request; no additional productions are anticipated.”
The records were obtained in response to a March 2022 lawsuit filed after the Department of Health and Human Services failed to respond to an August 2021 Freedom of Information Act (FOIA) request for records “submitted by Pfizer and BioNTech to the FDA, including BARDA, relating to ‘booster’ vaccinations for the SARS-CoV-2 virus.”
Biomedical Advanced Research and Development Authority, BARDA, has been heavily involved with the development of the Covid-19 vaccine. According to its website: