By vvital @Shutterstock
At NoMoreFakeNews.com, Jon Rappoport details the race from “emergency use authorization” of experimental vaccines to a “full approval”, and how its all happening behind closed doors. He writes (abridged):
The fix is in.
We’re racing from “emergency use authorization” of experimental vaccines to “full approval.” Boom.
Despite the promise of “transparency” prior to giving full approval to the COVID vaccines, the FDA is set to give its final green light this week. It’s a slam-dunk.
And there is NO public hearing.
This means the vaccine marketing/intimidation/mandate campaigns will ramp up much higher. “Well, now there is NO reason for anyone to refuse the shot. The FDA states it is completely safe and effective.”
Obviously, the FDA didn’t want to allow even mainstream “experts” to speak in a public hearing before approval; the agency is running a very tight ship. No slip-ups. No defections.
“Kim Witczak, a drug safety advocate who serves as a consumer representative on the FDA’s Psychopharmacologic Drugs Advisory Committee, said the decision removed an important mechanism for scrutinising the data.”
“’These [FDA] public meetings are imperative in building trust and confidence especially when the vaccines came to market at lightning speed under emergency use authorisation,’ she said. ‘The public deserves a transparent process, especially as the call for boosters and mandates are rapidly increasing. These meetings offer a platform where questions can be raised, problems tackled, and data scrutinised in advance of an approval’.”
“Witczak is one of the more than 30 signatories of a citizen petition calling on the FDA to refrain from fully approving any covid-19 vaccine this year to gather more data. She warned that without a [public FDA] meeting ‘we have no idea what the data looks like’.”
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