A hearing is scheduled in a case brought by a whistleblower who confirmed that violations occurred during the #Pfizer-BioNTech #COVID19 vaccine clinical trial.
Ventavia allegedly failed to properly report adverse events and keep all participants blinded.
https://www.theepochtimes.com/hearing-on-pfizer-clinical-trial-violations-set-to-take-place_5071138.html
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Ventavia allegedly failed to properly report adverse events and keep all participants blinded.
https://www.theepochtimes.com/hearing-on-pfizer-clinical-trial-violations-set-to-take-place_5071138.html
Subscribe ➡️⬇️➡️ @naomirwolf
The Epoch Times
Hearing on Pfizer Clinical Trial Violations Set to Take Place
The legal case brought by a whistleblower from Pfizer’s #COVID19 vaccine trial has been dismissed by a judge.
Brook Jackson, who worked for #Pfizer contractor Ventavia Research Group, did not prove violations of the False Claims Act, the judge ruled.
https://www.theepochtimes.com/pfizer-covid-19-vaccine-trial-whistleblower-case-dismissed-by-judge_5165422.html
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Brook Jackson, who worked for #Pfizer contractor Ventavia Research Group, did not prove violations of the False Claims Act, the judge ruled.
https://www.theepochtimes.com/pfizer-covid-19-vaccine-trial-whistleblower-case-dismissed-by-judge_5165422.html
Subscribe ➡️⬇️➡️ @naomirwolf
The Epoch Times
Pfizer COVID-19 Vaccine Trial Whistleblower Case Dismissed by Judge
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Report 87: In Early 2021, #Pfizer Documented Significant Harms and Deaths Following Vaccination with Its mRNA COVID Vaccine. The FDA Did Not Inform the Public.
https://dailyclout.io/pfizer-documented-significant-harms-and-deaths-the-fda-did-not-inform-the-public/
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https://dailyclout.io/pfizer-documented-significant-harms-and-deaths-the-fda-did-not-inform-the-public/
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DailyClout
Report 87: In Early 2021, Pfizer Documented Significant Harms and Deaths Following Vaccination with Its mRNA COVID Vaccine. The…
INTRODUCTION “5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of PF-07302048 (BNT162b2) Received Through 28-Feb-2021,” Pfizer’s post-marketing report, a required U.S. Food and Drug Administration (FDA) compliance document, is one of…