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COVID-19 Was a Concerted Effort by the “Global Cabal” to Control the Population ...

But now, four years hence, as the general picture has clarified itself, anyone with a sentient eye or ear not wedded to mainstream pulp can conclude that there never was a genuine pandemic, there never was a need to lock and shut down the entire world, and there never was or will be a need to inject billions with a gene-altering concoction that has hurt and killed too many to pass muster as a real and viable vaccine.

We can further conclude that the preposterously tremendous control over people exhibited by the roll-out of the covid campaign, and the submission of people to the evisceration of their unalienable rights — these were not organically evolved developments, but consequences of a highly orchestrated deployment of power.

In short, all things covid was a strategically planned operation — a war-crime — the likes of which are unprecedented, and the consequence of which is to move the world towards some kind of autocratic fiefdom wherein we ‘little people’ surviving the first waves of the onslaught will be subjugated to the whims and directives of The Few.

"It's just pretending, to get people to take poison, thinking that it's medicine..."

Katherine Watt lays out the seizure of power to enact Biomedical Fascism in the USA. The Covid-19 Operation in plain English: Interview with Peter and Ginger Breggin excerpts

It’s really a Constitutional Crisis
KW - So, the heart of it, in my view, is that what's being presented as a public health emergency, and as a pharmaceutical product, is actually not either of those things.

It's really a constitutional crisis. And it's been a constitutional crisis since long before it sort-of emerged on the scene in the beginning of 2020. Because the constitutional crisis is based in changes in US law that make it possible for the federal government to carry out biological attacks on the population, through the states, through biological products, like vaccines, and through emergency conditions and emergency orders, like the ones that came out during COVID.

Because really, what they're trying to do is injure and kill a lot of people here and around the world without getting caught, without getting stopped, without people seeing that that's what it is.

And what their overarching goal is to do is to concentrate power first in the federal executive branch in the United States, and then pass it over to the United Nations, the World Health Organization and whatever successor globalist organizations and institutions they develop. ...

So it's a joint project, joint deception project, between military leaders, FDA leaders, CDC leaders and corporate
KW - We don't actually know what's in any of the injections, because the way that the laws were rewritten, they never had to disclose the ingredients. And they never had to allow independent testing to confirm whatever they wanted to claim was in the ingredients.

So, I think some of the studies that have been done trying to, like, reverse engineer it and examine it, from people who diverted product out of the military supply chain and investigated [found], yes, there are mRNA components. There are LNP [lipid nanoparticle] components. There are lots of other components that we don't actually know. And there is no standardization among them.

And I would also say that it's not that the FDA is doing nothing. The FDA is an active complicitor [accomplice] in the performance that's being done. And without their participation, it would not have been able to move forward, because they had to be there pretending that there is a regulatory structure that applies to these products and pretending that they were applying it, so that people would think that the products were regulated and take them.

If they [FDA] had not been involved at all, if Pfizer had just come out by itself and said "We've made this thing. We're not going to tell you what's in it. We want you to take it. It's free," people would not have done it in the way that they did because the FDA was involved in the fraudulent way that it was involved.

So it's a joint project, joint deception project, between military leaders, FDA leaders, CDC leaders and corporate — Pfizer, Moderna, J&J, all of the other subcontractors and contractors that have produced components of countermeasures, or actual countermeasures. ...

Once those conditions are in place, the use of the product doesn't require informed consent.
One of them I found relatively early, a couple of years ago, that's 21 US Code 360bbb-3(k). And that's the one that says "use" of the EUA products "shall not constitute clinical investigation."

And so that's the law that basically said, under these specific conditions of public health emergencies, which are declared by the HHS Secretary unilaterally, they're not reviewable. They're not reversible by anyone other than the HHS Secretary [42 USC 247d-6d], to the extent that states and courts defer to these illegal laws.

Once those conditions are in place, the use of the product doesn't require informed consent. It doesn't involve real institutional review boards. There are no real review procedures at the FDA. Everything they do is just a pretense. Because the use is really for this other purpose, which is to injure and kill people without people finding out, or without people stopping it, without people being held criminally or civilly liable.

And that's the piece that came in with the PREP Act in 2005 [and Project Bioshield Act in 2004].

And then, the other one that I found much more recently relates more to the biological product licenses, "biologics license applications," called BLA. And that program dates back to some major revisions. It started in 1944, with the whole Public Health Service Act. There were some major revisions in 1973.

And then, just before they were about to launch this covert attack, using biological products that are unregulated -- that are actually poisons, but calling them medicines, through the Federal Register [84 FR 12505, April 2, 2019], making revisions to regulations [21 CFR 600.20, 21 CFR 600.21, 21 CFR 600.22] that are related to 42 US Code 262, which is the biological products section, they set it up so that there would be no specific time intervals for inspections of production facilities making biological products. There would be no specific enumerated duties for inspectors to visit the plants, take samples of the products, test the samples, apply regulatory enforcement actions.

And so that piece is a piece that becomes more relevant when you look at the things that other people talk about, as far as [claiming] "FDA did license Comirnaty in August of 2021."

Actually, they did not. Because that whole biologics license application or BLA process was corrupted just as the emergency use authorized program was corrupted.

They're written to make it possible to market and use poisons, calling them medicines...

Full Podcast here:

https://www.americaoutloud.news/the-fdas-sham-support-of-poisoning-the-american-public/