Urgent: on June 28, the ‘Future Framework” will be voted on, and if approved, all reformulated Covid-19 shots will skip clinical trials.

The ‘Future Framework” being voted on June 28th rigs the Covid-19 v@xxine regulatory process by taking the ‘flu strain selection process’ that fails every year and applying it to future (reformulated) C 0vid-19 shots. (See approving FDA member’s emails at the end of this email).

The FDA authorized Covid-19 shots for kids on June 14 and 15 and the “Future Framework” means shots that will be given to kids by fall will be the reformulated shots that skipped clinical trials.

Federal bureaucrats with financial conflicts of interests will then choose which SARS-C oV-2 variants to include in a yearly (or twice yearly) C ovid-19 shot. In the process, all future C ovid-19 shots will be deemed automatically ‘safe and effective’ without further clinical trials because they are considered ‘biologically similar’ to existing C ovid-19 shots.”
This the most reckless plan in the history of public health. This is clear proof that the FDA has completely abandoned science and its duty to protect the public.

What does the FDA have to say for itself!? The FDA released briefing document which is less than 20 pages 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are pre-prints or from the CDC’s in-house newsletter Morbidity and Mortality Weekly Report (MMWR) which means they are not peer-reviewed.

What you can do: Submit formal comment to regulations.gov.

(P.S. There are a quadrillion x quadrillion viruses and only a handful evolve slowly enough to be candidates for a vaccine. Viruses that evolve rapidly like SARS-CoV-2, the common cold, or HIV are bad candidates for a vaccine which is why all previous attempts to develop a vaccine against coronaviruses have failed (they never made it out of animal trials because #alltheferretsdied). Read more from Toby Rogers and CHD Defender.

Words that you will NOT find in the FDA “Future Framework” briefing document:

The FDA is literally not looking for many important real-life scenario possibilities (following the $cience indeed)!

To base the entire future of COVID-19 shots on a document the equivalent of a C-undergrad term paper is madness.

It’s a monetary decision. Pfizer and Moderna’s mRNA Covid-19 shots that they are making over $50 billion a year off of do not stop infection, transmission, hospitalization, nor death from the SARS-CoV-2 virus. Everyone knows this.

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Below are the email addresses of everyone at the FDA/VRBPAC. Share your own story or copy and paste the message below.

Subject line: All reformulated COVID-19 shots MUST go through proper clinical trials

The safety and efficacy of all reformulated COVID-19 shots must be evaluated through:

Large (50,000+ person) double-blind randomized controlled trials with inert saline placebos conducted by an independent third party. The treatment and control groups must be followed for life to monitor adverse events and all-cause mortality (no more wiping out the control group after 6 months to hide bad outcomes). We also demand greater than 90% efficacy against infection with less than 0.1% Grade 3 or higher adverse events; proper monitoring for carcinogenesis, mutagenesis and impairment of fertility; and immediate release to the public of all clinical trial documents submitted to the FDA.