How the US Government (FDA, DOD) removed the requirement for informed consent for EUA Countermeasures. <~ Due Diligence and Art

Criminals do not follow laws. They write them.

SASHA LATYPOVA MAY 20, 2024 READ

I wanted to add some information to a recent post by Katherine Watt: email answer to Bill Marshall (Judicial Watch). I agree with Katherine that both “aproved” (BLA) and EUA versions of covid shots are fake and poisonous. This applies to all of the 400+ covid products on the market – all of them are Emergency Use (EUA) only.  The most important thing about EUA status – it is non-investigational by law (Para 564 of FDCA).  Most people do not fully grasp the meaning of this.  While a chemical entity is classed as a non-investigational entity, it can never become a medicinal product in the ethical meaning of medicine, i.e. to treat, deliver some therapeutic benefit while minimizing the risk.  That is completely out of the question for an EUA.  It can never be used in a real clinical trial, because a clinical trial is a legally safeguarded investigation in humans.  Since no clinical trials are possible, no FDA approval (BLA) is possible as BLA by law requires safeguarded clinical trials with informed consent. 

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About michael burgwin

A child of the peace and antiWar movements, a Truther with self-diagnosed Opposition Defiance Disorder, formerly politically liberal tho now politically marooned, and Post-Doomer, on any issue, I trend to the conspiracy side, sort through the absurd, fantastical and insane, until I find firm ground usually located just the other side of the censorship firewall of propaganda and orthodoxy, dogma, and other either / or thinking.
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