A report from the Subcommittee on the Administrative State, Regulatory Reform, and Antitrust claims the Biden administration was the main impetus behind the FDA’s decision to fast-track an experimental mRNA drug for Covid-19, despite knowing full well they would push for vaccine mandates.
One of the members of congress behind the report, Subcommittee Chairman Thomas Massie (R-KY) accused the FDA of cutting corners to enable the Biden administration to more hastily enact the Emergency Use Authorization (EUA) used to justify the vaccine mandates. Massie said, “Exposing and acknowledging mistakes that were made is a necessary step toward restoring integrity and trust in our regulatory agencies.”
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Excerpt from amgreatness.com
A new report from the House of Representatives claims that the Biden Administration repeatedly pressured the Food and Drug Administration (FDA) into speeding up the approval of the Chinese Coronavirus vaccine developed by Pfizer.
According to the Daily Caller, the staff report from the Subcommittee on the Administrative State, Regulatory Reform, and Antitrust alleges that the FDA did not follow the usual regulatory guidelines when it came to approving the Pfizer vaccine. As such, when the FDA gave its approval to the vaccine, it allowed the Biden Administration to more quickly issue a mandate forcing federal workers and active duty troops to take the Pfizer vaccine or else risk losing their jobs.
In a statement issued by the House Judiciary Committee, which oversees the subcommittee in question, the committee further explained that the Biden Administration intended to “fully approve the Pfizer vaccine through the Biologics Licensing Application (BLA) process.” Although this process normally takes “ten months to a year,” or “six to eight months” if it’s a priority, the approval of the Pfizer vaccine took less than four months after Pfizer first filed its application.
