Vaccines against Covid 19 is biological weapon? Source: (https://bit.ly/3Bt3ELs) For anybody paying attention (and is also capable of simple arithmetic), it is now crystal clear that the negative effects of the COVID-19 "vaccines" far, far, far, far outweigh any benefits they ostensibly provide. (If they even provide any, considering their tendency to cause negative efficacy.) But the truth behind the experimental injections is far darker and more twisted than a completely out-of-whack risk-reward ratio. On the contrary, as pharma industry insider Sasha Latypova outlines in her presentation below, it turns out the injections are not actually pharmaceutical products at all. Instead, they are military products. And ones that Latypova claims - with overwhelming supporting evidence - behave as a literal bioweapon. Latypova, a serial pharmaceutical entrepreneur who spent more than 25 years in the pharmaceutical industry during her career - working with over 60 pharma companies all over the world, including Pfizer - has been delivering one bombshell announcement after another lately regarding the COVID-19 "vaccines." One of the biggest of which has been the fact that the U.S. Department of Defense (DoD) - and not pharmaceutical companies like Pfizer and Moderna - has ultimately been responsible for the COVID "vaccines'" manufacturing and distribution. The latter step occurring after the injections go through what Latypova refers to as the DoD "black box." In this relatively new presentation, which she recently posted to her BitChute channel dubbed Team Enigma, Latypova outlines how exactly the DoD has orchestrated the rollout of the COVID injections from manufacturing to distribution. Injections that she claims, and shows, are "toxic by design" due to their employing "mechanisms of injury," such as forcing a recipient's body to produce a literally unidentifiable version of the SARS-CoV-2 spike protein. The pharma industry veteran goes into more detail than in any of her other presentations so far regarding the covert DoD operation, particularly in regards to how it's been enabled through changes in federal law over the past several decades. Key amongst those legal changes were several from 1997, when Congress passed two laws including the FDA Modernization Act and The National Defense Authorization Act, which, combined, allow for implementation of an Emergency Use Authorization (EUA) for a given medical product. Which, in turn, (as Latypova notes) "gets rid of the FDA's safety and efficacy regulations and allows [the] FDA to issue emergency use authorizations for certain products which they deem required." Along with the federal legal changes in '97, Latypova also highlights the implementation of 10 U.S. Code § 4021, which amended the Other Transaction Authority (OTA) of the DoD. As Cornell's Legal Information Institute describes, OTA gives "The Secretary of Defense and the Secretary of each military department [the ability to] enter into transactions (other than contracts, cooperative agreements, and grants) [in order to carry] out basic, applied, and advanced research projects." Cornell's Institute adds "The authority under this subsection is in addition to the authority provided in section 4001 of this title to use contracts, cooperative agreements, and grants in carrying out such projects." In other words, 10 U.S. Code § 4021, implemented under the Obama Administration in 2015, allows the DoD to order "undisclosed military prototypes" from private manufacturers, such as pharmaceutical companies. Not only that, but it allows the private contractors making the DoD's military prototypes to completely avoid any kind of manufacturing, safety, or efficacy disclosures. The last keystone of the "pseudo-legalization" of EUA-covered military "countermeasures," Latypova notes, was the Public Readiness and Emergency Preparedness Act - or PREP Act - which allows the head of the Department of Health and Human Services (HHS) to unilaterally issue declarations recommending the manufacture, testing, development, distribution, administration, and use of one or more countermeasures. Shortly before the supposed SARS-CoV-2 "global pandemic" (which the WHO literally refers to as a PHEIC or "fake" emergency, read more about that immediately above), Latypova notes the PREP Act was amended, "very thoroughly" exempting "anyone participating in this program, in this activity, in this bioterrorism program, from any liability from lawsuits [or] from injuries and deaths caused by these actions." Subsequently, the Trump administration declaring a national public health emergency in 2020 - one that's been continually extended by the Biden administration - has allowed for the DoD to rollout the fully legally immunized COVID injections. Latypova notes the public health emergency must continue in perpetuity, as "this is the keystone that holds all of this criminal structure together." Latypova refers to this legal framework as a "criminal structure," in part, because these "undisclosed military products" can literally be weapons; including "biological, chemical, radiological, or nuclear" weapons. The pharma insider adds "all of [these weapons] can fall under the vaguely defined terms [of the DoD's OTA contracts]." Key to initiating the ability for the DoD to rollout these legally immunized, largely undisclosed products, Latypova shows, is the HHS Secretary declaring a public health emergency. On top of this pseudo-legal criminal structure, Latypova notes the perpetrators of this COVID scam - including the DoD, Pfizer, Moderna, etc. - had "ample means, motive, and opportunity through… OTA contracts to ensure that no evidence ever becomes available." Latypova adds there has also been "huge media collusion to ensure that there is no evidence; suppression of evidence. Censorship. Deletions. Deplatforming. Hiding. And lying and obfuscation." Most critically, Latypova shows how EUA "medical" countermeasures, "once designated as such by the Secretary of Health and Human Services, shall not be considered to constitute a clinical investigation." This is why the FDA "approving" the COVID injections has simply been a theatric performance. Simply a farce with no legal or regulatory impact on the rollout of the undisclosed military products (i.e. the COVID injections). "[The COVID injections] are not actually clinical investigational products," Latypova says, "meaning that they're not subject to any normal pharmaceutical regulatory rules. And that's why they're not countermeasures… you can only say what they're not. And we definitively can say here that [the COVID injections] are not pharmaceutical products." The pharma insider clarifies that "when [the] FDA goes on media and says, 'Oh, you know, we reviewed COVID-19 vaccines and they're safe and effective, they're lying in many, many ways… ." The first way the FDA is lying is that the agency is talking about the injections as if they have regulatory authority over them, when it does not. Likewise, the COVID "vaccine" development and approval "could be named [after] a movie or a theater production or show, [as] it's a performance…" Latypova says. She adds "there is no vaccine development and approval because these products are not pharmaceuticals. They're not vaccines, they're countermeasures under EUA, under public health emergency, they're not subject to any regulation. Especially not pharmaceutical regulation." This explains the very strange use of the word "demonstration" in the DoD contracts with the likes of Pfizer, Moderna, et al. Latypova adds the use of "demonstration" legally makes any regulation by the FDA in regards to the COVID-19 vaccines - including their clinical trials - utterly moot. "You cannot do a clinical trial for something that… cannot be an investigational clinical product. Also, the Good Manufacturing compliance was not ordered by these contracts because it's not possible because the COVID injections are not a pharmaceutical product. What [the] FDA is really doing is they're impersonating… regulators and lying to the public." As a result of the DoD being solely responsible for the manufacturing and delivery of the COVID injections, "no regulators in the world know what protein is actually expressed by these mRNA injections." Apparently Pfizer, Moderna, and other ostensible producers of the COVID injections are claiming they're injecting people with the mRNA code for the SARS-CoV-2 spike protein, when, in fact, it's not publicly known what's being injected, except for the fact that it is not the SARS-CoV-2 spike protein. Latypova says this is definitive, as the only thing that's known about the produced spike protein is that it is far heavier (in terms of molecular weight) than the SARS-CoV-2 spike protein. Furthermore, the manufacturers of the COVID injections (around the world) say it's not even possible to figure out what kind of protein the injections are developing in the human body. As far as the national COVID-19 response plan, Latypova notes it was the National Security Council (NSC) that developed and implemented it. The pharma insider notes that "since 2018 at least we had a pandemic action plan that was called PanCAP, and that pandemic action plan stated that HHS was actually in charge of pretty much everything… [and] did not include stupid things like lockdowns. And would not mandate masks on everybody." Those were "more reasonable and normal and science-based actions that were recommended in those plans." In 2020, the NSC's PanCAP told "a completely different story." In that version, the NSC was in charge of emergency public health policies. This is incredible, as the NSC does not even include public health agencies typically involved with public health emergencies. On the contrary, it mostly consists of national defense and intelligence leaders. "So now, all of the sudden, since 2020 [these NSC council members have been put] in charge of COVID policy." While the NSC was in charge of formulating the COVID policy, Latypova notes it was FEMA who ostensibly implemented it because Trump declared a national health emergency under the Stafford Act. FEMA, however, was "only a figurehead role… [and has been] visible, ceremonial, but unimportant…" Latypova adds "the HHS [has only been] in the information and propaganda role." After Trump invoked the Stafford Act he initiated Operation Warp Speed (OWS), which was brought in to develop the COVID injections and other countermeasures such as therapeutics and diagnostic tools. Latypova notes OWS was sold as a collaborative effort between HHS and the DoD, "but the actual organization structure" shows it was the latter agency that was entirely in charge. Latypova shows an organizational chart revealing the decision-making structure behind OWS, with the DoD in the most executive role. The HHS was only the "chief science advisor." This "makes it very clear that the Department of Defense [was] in charge of the whole thing,".