Breaking: WHO Behind FDA Scheme to Skip All Future Clinical Trials for COVID Vaccines, by Toby Rogers, Ph.D.

If you thought that present pharmaceutical company, NGO, and regulatory agency skullduggery were bad, wait until you read this article. They’re going for new lows. From Toby Rogers, Ph.D., at childrenshealthdefense.org:

The “Future Framework” is coming from the World Health Organization, and the Bill & Melinda Gates Foundation is the biggest voluntary contributor to the WHO, so Gates is likely directing the play.

Introduction: The FDA always rigs the game on behalf of Pharma

Late Friday afternoon, the FDA released its agenda for the Vaccines and Related Biological Products Advisory Committee (VRBPAC) meeting that will vote on the Orwellian “Future Framework” on Tuesday, June 28.

Then on Saturday morning, the FDA released a briefing document in connection with this scheme to end science as we know it in connection with future COVID-19 shots. (Much appreciation to the brilliant James Roguski for alerting me to these documents.)

In this article, I will explain what is in the briefing document, what is likely to happen at the meeting and what can be done about it.

The FDA’s ‘Future Framework’ briefing document

The briefing document is 18 pages of text, 1.5 line spacing, with just 19 references — 9 of which are pre-prints or from the CDC’s in-house newsletter Morbidity and Mortality Weekly Report (MMWR) which means they are not peer-reviewed.

Any true believer in The Narrative(TM) could have written this in a few hours. To base the entire future of COVID-19 shots on this glorified undergrad term paper is madness.

As I predicted, even though the April 6 meeting was presented as an exploratory initial conversation that reached no conclusions whatsoever, the “Future Framework” is now being presented by the FDA as a done deal, fait accompli, you’d have to be crazy to insist on proper safety studies.

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