New texts reveal Fauci, Gates ignored safety studies, broke the law

More proof Fauci and Gates wilfully ignored the warnings that covid vaccines were causing huge damage and broke the law 

From media

A newly released email suggests that the nation’s top vaccine regulator encouraged Dr. Anthony Fauci and Dr. Francis Collins to leverage billions in scientific research dollars to study COVID vaccine side effects — but they never followed through on her request.

In the spring of 2021, Janet Woodcock, then head of the Food and Drug Administration (FDA), wrote to the leaders of the National Institutes of Health — the country’s leading funder of medical science — to encourage a study into reports she had received of adverse events after COVID-19 vaccination. Woodcock had received many of these reports from “healthcare professionals,” she wrote in the email released by Republican Wisconsin Sen. Ron Johnson and obtained from Fauci’s government email.

“The symptoms do not fit together into a distinctive syndrome and most are not easily quantifiable or evaluated with standard laboratory testing,” she wrote in the May 27, 2021 correspondence. “Clearly during mass vaccination you will get a lot of psychological reactions and it is hard to sort these things out. But the peoples’ main complaint is that no one takes them seriously, no one knows how to treat them, and there is no effort to study this.” (RELATED: ‘This Is All Data Free’: Fauci’s Texts Reveal Concerns About COVID Vaccines And Miscarriages)

Woodcock said that these studies should be undertaken even if the vaccine makers would not support them.

“I doubt the industry would support, for obvious reasons,” she wrote in the email. “But my experience is, that if you let a problem fester, then it will come back to bite you later and you are not prepared.”

https://dailycaller.com/2026/08/16/anthony-fauci-janet-woodcock-email-covid-vaccine-side-effects/

From AI

studying the safety and side effects of COVID-19 vaccines was legally obligatory for manufacturers under U.S. federal law and U.S. Food and Drug Administration (FDA) regulations before and after authorization.

Key Governing Rules and RegulationsFederal Food, Drug, and Cosmetic Act (FD&C Act): Empowers the FDA to oversee the safety, effectiveness, and labeling of drugs and biological products.

Code of Federal Regulations (Title 21, 21 CFR Part 312): Governs Investigational New Drug (IND) applications, requiring clinical trial sponsors to systematically track, evaluate, and report adverse events and side effects during human testing.21 

CFR Part 50 and Part 56: Mandates human subject protection, rigorous informed consent regarding potential risks/side effects, and Institutional Review Board (IRB) oversight.

Emergency Use Authorization (EUA) Statutory Standards (Section 564 of the FD&C Act): 

Required the FDA to determine that the known and potential benefits of the vaccines outweighed their known and potential risks based on safety data submitted by manufacturers.Post-Marketing Surveillance Requirements: Under federal oversight, manufacturers were legally mandated to continue safety monitoring and conduct post-approval/post-authorization studies to track rare adverse events like myocarditis.