02/15/2023 / By Ethan Huff
After Congress passed the Public Readiness and Emergency Preparedness Act (PREP Act) back in 2020, things changed for the worse at the U.S. Food and Drug Administration (FDA) in terms of the standards used to authorize and approve vaccines, biologics, and other pharmaceutical drugs.
All of the certified Good Clinical Practices (GCP) that were followed prior to 2020 went out the window at the height of the Wuhan coronavirus (Covid-19) scamdemic to pave the way for warp speed drug approvals on the fly, which is exactly what happened with Operation Warp Speed.
(Related: Check out our earlier coverage about the PREP Act to learn more about this heinous law and what it did to exempt the vaccine industry from legal liability for injuries and deaths caused by covid “vaccines”.)
Whistleblower Brook Jackson brought to light many of the blatant violations of GCP in Pfizer’s human clinical “trials” for its messenger RNA (mRNA) shot, which we now know is both dangerous and ineffective. Ventavia, the Pfizer partner that held the trials, knew full well about the violations at the time of the trials.
After Jackson blew the lid on the whole operation, Ventavia went into attack mode. It vilified the victims of Pfizer’s lethal injections who are now suffering or dead because of getting jabbed, as well as arranged for Jackson to be fired for telling the truth.
The following bullet points highlight the observations that Jackson made while at Ventavia, which she included in her whistleblower complaint:
Had the old, pre-PREP Act rules still been valid at the times of these fraudulent trials, none of the aforementioned issues would have been tolerated. In fact, the entire clinical trial operation would have been halted immediately.
Instead, the trials proceeded as normal, despite all the corruption, and were used to later justify mandating covid injections on millions of Americans who otherwise would have just said no to these deadly drugs, as the late First Lady Nancy Reagan once urged.
During the emergency use authorization (EUA) farce, Pfizer, in conjunction with the Department of Defense (DoD), submitted Wistar rat data to fake FDA reviewers as part of the package. That clinical trial “study” included admissions by Pfizer and the DoD that no assessment would be made of pharmacokinetics, pharmacodynamics, biomarkers or genetics with regard to the injections.
“The primary purpose of all the statutory, regulatory changes and guidance document revisions year after year, page after page, is to keep people from, first, understanding the war crimes as war crimes, and – if people do figure it out – keep them chasing their tails trying to find the FDA loophole that the war criminals somehow failed to close, through which somebody might someday be able to get them to stop killing us,” writes Katherine Watt for Bailiwick News – be sure to read her full assessment of the situation.
More news stories like this one can be found at FDA.news.
Sources for this article include:
big government, Big Pharma, Censored Science, corruption, COVID, deception, EUA, fake, faked, FDA, pharma fraud, PREP Act, research, science deception, vaccination, vaccine wars, vaccines, whistle-blower
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