Republicans Press FDA for Testimony on Rushed COVID-19 Vaccine Approvals
Republicans on the House Select Subcommittee on the Coronavirus Pandemic are seeking answers after recently released emails indicated that the U.S. Food and Drug Administration (FDA) had rushed the approval of COVID-19 vaccines and boosters to accommodate vaccine mandates.
“According to new internal U.S. Food and Drug Administration (FDA) communications, it appears the Biden Administration may have bypassed, compressed, and possibly compromised the longstanding process for awarding a full biologics approval to a vaccine,” the legislators wrote in a March 10 letter (pdf) to FDA Commissioner Robert Califf.
“This effort may not have been to save lives, but concernedly to provide cover for implementing and enforcing vaccine mandates across the country,” they charged.
As first reported in January, the emails in question showed that, in 2021, the FDA’s Office of Vaccines Research and Review (OVRR) was being pressured by agency officials to speed up its review of the Pfizer vaccine despite the concerns of some staff members
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