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The fed gov’t shields Pfizer from liability. Gives it billions of dollars. Makes Americans take its product. But won’t let you see the data supporting its safety/efficacy. Who does the gov't work for?
originally posted by: myselfaswell
a reply to: HawkEyi
This is good news, now we know we'll never be able to provide informed consent for 55 years.
originally posted by: RazorV66
a reply to: HawkEyi
Yeah the government can eat my shorts.
Good luck to everyone that has already taken their fake “vaccine”
...The FDA has proposed to produce 500 pages per month which, based on its calculated
number of pages, would mean it would complete its production in nearly 55 years – the year 2076.
Until the entire body of documents provided by Pfizer to the FDA are made available, an
12 See 21 CFR § 601.51(e).
13 Reports have recently surfaced that the FDA was aware of concerns about unsound practices in connection with
clinical trials for the Pfizer Vaccine, but that FDA failed to properly investigate these claims.
Page 11 of 14
appropriate analysis by the independent scientists that are members of Plaintiff is not possible.
Would the FDA agree to review and license this product without all the documents? Of course
not. These independent, world-renowned scientists should be provided the same forthwith.
The entire purpose of the FOIA is to assure government transparency. It is difficult to
imagine a greater need for transparency than immediate disclosure of the documents relied upon
by the FDA to license a product that is now being mandated to over 100 million Americans under
penalty of losing their careers, their income, their military service status, and far worse.
It took the FDA precisely 108 days from when Pfizer started producing the records for
licensure on May 7, 2021,14 to when the product was licensed on August 23, 2021.
15 We assume,
as the FDA has stated, that it conducted an intense, robust, thorough and complete review and
analysis of those documents in order to assure that the Pfizer vaccine was safe and effective for
licensure. The FDA now has an equally important task of making those documents available to
the Plaintiff in this case and the public at large in at least the same timeframe.