Authored by Zachary Stieber via The Epoch Times (emphasis ours),
U.S. drug regulators acknowledged deviating from the normal vaccine approval process when dealing with Pfizer’s COVID-19 shot, according to newly disclosed documents.
Weeks after Pfizer and its partner BioNTech announced they started a rolling submission of documents for approval of their COVID-19 vaccine, a U.S. Food and Drug Administration official penned a memorandum authorizing the release of a Biologics License Application (BLA) number for the shot even as regulators weighed whether to approve the BLA, one of the documents shows.
“This deviation from our normal practice is done to facilitate product labeling and distribution and is consistent with other Center practices to facilitate vaccine delivery during the declared Public Health Emergency,” Christopher Joneckis, the FDA’s associate director for review management, wrote in the June 17, 2021, memo. “When providing the license number, we should communicate that this license number does not constitute any determination by FDA on the application.”
Joneckis said the decision stemmed in part from the FDA having granted Emergency Use Authorization (EUA) for the shot in late 2020. That means the FDA “is familiar with and has reviewed much of the information provided in the BLA application,” which primarily consisted of data used in the application for emergency clearance, he said.
EUAs can be granted if a public health emergency has been declared and the FDA determines it’s “reasonable to believe” that the vaccine or other product in question “may be effective” in preventing, diagnosing, or treating the disease or condition caused by the public health threat. BLAs require a higher threshold of evidence, demonstrating that a product is “safe, pure, and potent.”
A separate document made public this week showed that the license number was given to Pfizer even though no approval decision had been made after Pfizer requested it.
“The Applicant requested a U.S. License Number for BioNTech Manufacturing GmbH with agreement that they will not use it until after the BLA is approved,” the document, a summary of a June 29, 2021, FDA meeting discussing Pfizer’s application, stated.
The summary noted that Joneckis wrote the memo authorizing the release of the number “in advance of the typical notification in the approval letter.” After that, the FDA “generated the license number which will be provided to the Applicant, after filing, in an email message.”
The FDA granted a BLA to Pfizer’s vaccine for individuals 16 and older on Aug. 23, 2021. The vaccine was later approved for children as young as six months of age. The FDA has also authorized or approved multiple boosters due to the vaccine performing poorly against newer variants.
The documents were released by the Informed Consent Action Network (ICAN), which successfully convinced a court to order the FDA to produce documents related to its actions on the COVID-19 vaccines after the agency had claimed it would take decades to do so. The government has been providing ICAN documents in response to the suit and Freedom of Information Act requests.
Aaron Siri, a lawyer representing the network, told The Epoch Times in an email that the new documents are “another piece of evidence that supports that licensure of this product quickly became a foregone conclusion.”
The FDA did not respond to a request for comment.
Advisory Committee Meeting ‘Not Needed’
The FDA only held one meeting with its advisory panel, the Vaccines and Related Biological Products Advisory Committee (VRBPAC), after Pfizer and BioNTech lodged their BLA request. That meeting focused on whether to clear vaccines for younger populations, and not the new application.
During the meeting, multiple panelists expressed confusion about when they would be consulted on any BLA requests.
Read more here...