On the continuing effort to fit a square peg (legalized manufacturing and use of biological weapons) into a round hole (FDA drug, device and biological product regulation).
Meryl Nass, promoting David Gortler’s work:
My reply:
It is not true that any Covid vaccines have been licensed.
All FDA activity that appeared to be license-related, pertaining to all biological products manufactured since May 2019, has been fraudulent, performative, charade, pretextual, and any other word or phrase that means not real, not substantive, not legally relevant.
And all biological product development, manufacturing and use since February 4, 2020, has had additional layers of non-regulation and liability exemption (license-to-kill) through the PHE-EUA-MCM-PREP structure and the Defense Production Act structure.
Feb. 9. 2023 - On the significance of 21 USC 360bbb-3(k): "use" of EUA products "shall not constitute clinical investigation."
Until litigants properly identify the toxic products as unregulated poisons, biochemical weapons, or other accurate terms, no court cases are going to move things along toward ending the 'vaccination' and 'biological products' programs in their entirety and bringing the medicalized mass murder chapter of American history to a close.
Litigation that erroneously identifies the toxic products as regulated biological products or vaccines is a waste of time and money, and only serves to extend the mass murder programs.
Update added Jan. 6:
Reader asked for some clarification on [this] post, including clarification from me, about what Meryl Nass knows, understands and writes or speaks about FDA’s functions during what I understand to be theatrical performances of ‘deadly global pandemics’ and biological product licensing and use.
I can’t address what Nass knows, understands, or how she expresses her views — only she can answer questions about those things.
My position is that everything FDA has done or said or written, regarding every biological product (including but not limited to vaccines, including but not limited to Covid-19 products) that is presented as having been manufactured and/or licensed since May 2, 2019, has been a lie, a fraud, a performance only.
Documents purporting to be regulatory documents, (BLA, EUA, all other classifications), are falsified documents (theatrical props) with no legal substance or enforcability or enforcement action, if the documents exist at all.
There are no applicable FDA regulations about non-adulteration, purity, labeling, testing, safety, efficacy or any other aspect of drug, device or biological product development, testing, manufacturing, labeling, or use, that apply to/can be enforced/have been enforced for any product presented as a Covid-19 countermeasure, or as a licensed biological product, whether for Covid-19, or flu, or RSV, or measles, or any other disease or condition.
