The FDA authorized Covid-19 shots for kids on June 14 and 15 and the “Future Framework” meeting

W3THEMEDIA:

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).
Federal bureaucrats with financial conflicts of interests will then choose which SARS-C oV-2 variants to include in a yearly (or twice yearly)

Covid-19 shot. In the process, all future Covid-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.

https://healthfreedomsummit.mykajabi.com/e/BAh7BjoWZW1haWxfZGVsaXZlcnlfaWRsKwgUiazBAQA%3D--a6d8691fff21778e2d781b7ca025461d18fd1684?skip_click_tracking=true&fbclid=IwAR1GrV8AIZzgomlpvaRrnWCcS20mWetuo-yeNvc07hadKnep-M66mSdWFNQ#

Vaccines and Related Biological Products Advisory Committee Meeting – 6/28/2022 https://www.youtube.com/watch?v=BFdzNUus_CE

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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.

sean.mccluskie@hhs.gov, commissioner@fda.hhs.gov, DeanofPublicHealth@brown.edu, Aux7@cdc.gov, Peter.Marks@fda.hhs.gov, Hong.Yang@fda.hhs.gov, Richard.Forshee@fda.hhs.gov, Huilee.Wong@fda.hhs.gov, Leslie.Ball@fda.hhs.gov, Doran.Fink@fda.hhs.gov, jerry.weir@fda.hhs.gov, hanae@bcm.edu, paula.annunziato@merck.com, adam.berger@nih.gov, hbernstein@northwell.edu, acohn@cdc.gov, anc0@cdc.gov, hjanes@fredhutch.org, hgans@stanford.edu, david.kim@hhs.gov, asmonto@umich.edu, offit@chop.edu, spergam@fredhutch.org, Jportnoy@cmh.edu, erubin@hsph.harvard.edu, erubin@nejm.org, ashane@emory.edu, swamy002@mc.duke.edu, fullerao@umich.edu, RandyHawkins@cdrewu.edu, officeofthepresident@mmc.edu, JYLee@uams.edu, ofer.levy@childrens.harvard.edu, wayne_marasco@dfci.harvard.edu, cmeissner@tuftsmedicalcenter.org, mrn8d@virginia.edu, stanley-perlman@uiowa.edu, mhsawyer@ucsd.edu, mew2@cdc.gov, jlessler@unc.edu