FDA - Lack of transparency issues

Something suspicious is happening in the USA, as the competent drug and food control body has asked a court not to release the documents related to the licensing of vaccines, before 2075!

As of Nov. 14, more than 256 million doses of the Pfizer vaccine for COVID-19 have been administered in the United States.

FDA asked a federal judge on November 15 to give him a deadline of 2076 δηλαδή 55 years… to fully disclose the documents in his possession related to the approval of the Pfizer - BioNTech vaccine for COVID-19.

FDA request was filed as part of a Freedom of Information Act (FOIA) lawsuit filed against it by a team of doctors seeking transparency in vaccines.

The court was told that the government has… 329,000 pages of documents in response to the FOIA request and proposed issuing 500 pages a month.

At this rate, FDA would release those files in less than 55 years.

Plaintiff, Public Health and Medical Professionals for Transparency (PHMPT), is a team of physicians and scientists, including Harvey Risch, Professor of Epidemiology at Yale School of Public Health.

The team filed the lawsuit after FDA rejected the request to expedite the publication of the files.

The plaintiff and the defendant failed to reach an agreement on the timing of the disclosure of all the documents, and so they ended up in court.

"FDA's promise of transparency is, to put it mildly, a pile of illusions," wrote Aaron Siri, whose company represents PHMPT in the lawsuit, in a November 17 post.

"It took FDA exactly 108 days from the time Pfizer filed the licensing files to the time the FDA licensed the Pfizer vaccine," Siri continued.

"FDA carried out a thorough and complete analysis of these documents, ie 329,000 pages, in order to ensure that the Pfizer vaccine was safe and effective for licensing.

While it was able to perform this evaluation of Pfizer documents in 108 days, it evaluated 329,000 pages in 108 days…. now it is asking for more than 20,000 days to make these documents available to the citizens of the world ".

FDA did not respond to a request for comment.

FDA licensed the Pfizer COVID-19 vaccine under the name Comirnaty on August 23, 2021, less than four months after Pfizer began submitting documents for full approval of the vaccine.

The approval of the license by FDA at the end of August led to an avalanche of vaccine orders in the private and public sectors.

One of the companies involved in testing the Pfizer vaccine earlier this month said it was investigating alleged problems brought to light by an informant who told the British Medical Journal (BMJ) that the tests had many issues including falsification of a lot of data.

The informant, named Jackson, notified the FDA and was fired within hours.

Jackson worked for Ventavia Research Group, which was managing several trials of the Pfizer vaccine in the fall of 2020.

According to the British Medical Journal, one of the oldest medical journals in the world, the FDA did not inspect Ventavia test sites, despite receiving notice.

FDA told The Epoch Times in an email earlier this month that while it could not comment on the Ventavia issue, "it has full confidence in the data used to support the Pfizer-BioNTech vaccine authorization for COVID-19 and the approval of the Comirnaty vaccine »

FDA risks to become an example of a non-transparent organization which does not respect its statutory goals!

In the light of the above mentioned information FDA credibility is at risk in front of the eyes of every intelligent medic who respects Hippocrates Oath and wants to safeguard his/her patients’ health!