Sasha Latypova is an ex-pharma employee and biotech expert. She has 25 years of experience in clinical research and regulatory approvals, and has worked with over 60 pharmaceutical companies, as well as the FDA. She is also part of “Team Enigma,” a team of doctors and researchers who have diligently worked to uncover what was in the Covid shots.
A short while back, Latypova was interviewed by Maria Zeee, of Zeee Media, and she brought forth information received through Freedom of Information requests that most will find disturbing, not the least of which is that Operation Warp Speed, with it’s military-sounding name, is, in fact, an operation run by our own Department of Defense.
Latypova reports that standard Good Manufacturing Practices (GMP), which is a set of laws meant to protect the public from harm, were not followed in the production of the “vaccines.” She reports her team’s analysis of the adverse events, post-injection, reported on the CDC’s VAERS website, revealed the variability in product, lot-to-lot, batch-to-batch, was thousands of times higher than what is expected from a well-manufactured product. Typically, that kind of variability would cause a product to be recalled immediately, just as car manufacturers recall certain makes and models. Not so with these synthetic injectables.
In fact, on January 18, 2021 (just two weeks after the full rollout of these shots), an organization in Orange County, California detected a problem with one of the lots of Moderna (which is unsurprising given that I just watched Ray Kurzweil brag that it only took two DAYS to produce the Moderna shots). They proclaimed there were too many “alllergic” reactions. This was reported on numerous outlets, including CNN. Then nothing happened. That lot continued to be distributed throughout the U.S. until it ran out at the end of March, 2021. From that Moderna lot, Latypova states: “I counted in VAERS system over 3000 adverse-event reports and 60 deaths. So, on January 18, 2021, they detect an issue and they do nothing and kill 60 people (at least; we know VAERS is under-reported). So after that occurrence, everything else should be considered intentional.” That Moderna lot was distributed throughout the world. Actions should have been taken by the regulators to halt their use. But nobody did anything. One of the reasons for this is that there are no actual regulators. Those we’ve seen claiming to be regulators are nothing more than posers paid to lie.
In preparation for all of this, the U.S. Government and DOD, over many years, put in place three specific elements to remove pesky safety regulations from injections: 1) they created “Other Transactional Authority,” which allows them to work with private companies to create prototypes of any number of things, do research, etc; 2) they classified the shots as “countermeasures,” which are emergency-use authorized; and 3) they had a “Public Health Emergency” declared. So when those three stipulations are met, no regulations apply whatsoever.
Then, Latypova further states, “The only standard for releasing/deploying them is: the sole discretion of the secretary of HHS.” If he deems that they “may” be effective, that is all that is required for their release. Azar conveniently created this law for himself in September of 2020, giving himself sole power and authority over any foods, medicines, testing and vaccines, stripping that power from the FDA. They had no say-so. So what the FDA has been doing all this time is acting.
The FDA has no role in regulating these products. None. And that’s the brazen fraud that has been committed against us all.
Further, Latypova shares that “U.S. Code 360 BBB(k) states: Emergency Use Authorized covered medical countermeasures, once designated as such by the Secretary of HHS, shall not be considered to constitute a clinical investigation.” So under this 1997 EUA law, amended in 2003, 2004, 2005, 2013, and 2017 (showing ongoing pre-planning) when HHS declares a public health emergency, then the secretary can use EUA-covered medical countermeasures. And when they do, it does not constitute a clinical investigation, meaning the FDA has no role whatsoever in regulating it.
So when they performed these clinical trials, it was all theatre. By law, these products can’t have a clinical investigation. So the trials we heard about were literally pretend clinical trials.
And while money has been a big reason for the plandemic — with 576 new billionaires having been minted during the manufactured crisis — the real reason for it is, according to Latypova, intentional infliction of death and/or injury on as many people as possible.
(In a separate video, Dr. Mike Yeadon, a research partner of Latypova’s, states that, despite the fact that he has never been religious, he can only deduce that, with the kind of planning that has been involved in this operation that has released toxic products into billions of people, that it could only.have been done by those who worship satan.)
Latypova rightly points out that if this were all just about money, the suppliers could just ship placebo in perpetuity, and no one would know the difference. The suppliers would make 10 times the money. But that’s not what was done because money wasn’t the primary goal. Death, mass injury, and surveillance-from-under-the-skin were the goals.
The nanotechnology Ray Kurzweil states is key to the transhumanism he thinks we should all embrace — with boosters required to “upgrade” — is now in untold billions of people. (Also, the fact that Kurzweil, Google’s Director of Engineering — Google being a major U.S Government/DOD contractor — was apparently present for the manufacture of some of the “vaccines” is telling.)
Finally, several years ago, I came across a document produced by the DOD in 2000, entitled “Joint Vision 2020,” which illustrated their stated goal for the year 2020 was “full spectrum dominance.” It states, “The label full spectrum dominance implies that U.S. forces are able to conduct prompt, sustained, and synchronized operations with combinations of forces tailored to specific situations and with access to and freedom to operate in all domains — land, sea, air, space, and information.”
Seeing that word “information” might not mean much until you realize that we simple humans are information. We are walking data covered in skin. And with the human genome project having been completed in the early 2000s, the “code” of humans was revealed. We are made up of ones and zeroes and, as such, are just as hackable as any other computer code. All that is needed is the software (provided by Autodesk) and access to our inner bodies (provided by nanotechnology — repeatedly proven to be present in the synthetic RNA injections).
So, it appears Operation Warp Speed led directly to the achievement of the DOD’s goal of full-spectrum dominance. And with that, the picture is perfectly clear.
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Ashley Hayes is a former business entrepreneur, patented inventor, researcher, and writer seeking to bring attention to the clearly-organized crimes of unlawful and corrupt law enforcement and fusion center personnel against innocent Americans and citizens worldwide, as well as crimes committed by military contractors via 21st century technology, and to the pandemic of child trafficking by those in power.
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