Global Research / Armed Forces Press
According to congressionally passed statutes, research of active laws, and extra details obtained through the Freedom of Information Act, the Department of Defense owns, implements, and oversees the COVID-19 vaccine program as a “Countermeasure” to foreign attack. While the public was bombarded with an orchestrated fear campaign, the U.S. Government managed the Covid response as a national security threat.
The Three-Legged Stool
Hello whyThe undercover operation was orchestrated utilizing three critical legal maneuvers:
1. Emergency Use Authorization EUA.
2. Prep Act,
3. Other Transactions Authority
President Trump declared a Public Health Emergency (PHE) on March 13, 2020, under the Stafford Act, putting the National Security Council in charge of the Covid policy.Covid-19 vaccines are “medical countermeasures” – a grey area of products that are not regulated as vaccines or medicines.
“They put the National Security Council in charge and treated it as an act of war,” said Latypova.
According to Operation Warp Speed/ASPR reports, the DoD ordered, oversaw, and tightly managed the development, manufacture, and distribution of Covid countermeasures, mainly utilizing the DoD’s previously established network of military contractors and consortia.
Department of Defense, BARDA, and HHS ordered all Covid countermeasures, including “vaccines” as prototype demonstrations of large-scale manufacturing, avoiding regulations and transparency under Other Transaction Authority. As prototypes used under EUA during PHE, Covid countermeasures, including “vaccines,” need not comply with the U.S. laws for manufacturing quality, safety, and labeling.
“The implication is that the U.S. Government authorized and funded the deployment of noncompliant biological materials on Americans without clarifying their “prototype” legal status, making the materials not subject to normal regulatory oversight, all while maintaining a fraudulent pseudo- “regulatory” presentation to the public,” said Latypova.
“Most incredible is the fact that current Laws enacted by the United States Congress appear to make the coverup actions LEGAL!”
Under the PHE, medical countermeasures are not regulated or safeguarded as pharmaceutical products (21 USC 360bbb-3(k).
The American people were led to believe that the FDA, CDC, and figureheads like Anthony Fauci oversaw the COVID-19 vaccine program.
Their involvement was an orchestrated information operation. All decisions concerning the COVID-19 vaccine research, materials acquisition, distribution, and information sharing were tightly controlled by the DoD.
Hundreds of Covid countermeasures contracts have been uncovered. Many disclosures are in redacted form. However, Latypova and Watt have found sources to fill in the details.
A review of these contracts indicates a high degree of control by the U.S. Government (DoD/BARDA). It specifies the scope of deliverables as “demonstrations” and “prototypes” only while excluding clinical trials and manufacturing quality control from the scope of work paid for by the contracts. To ensure that the Pharma is free to conduct the fake clinical trials without financial risk, the contracts include the removal of all liability for the manufacturers and any contractors along the supply and distribution chain under the 2005 PREP Act and related federal legislation.
Why is no action by regulators or courts?
According to Latypova and Watt, a combination of recently passed legislation and executive orders make it LEGAL to LIE! The HHS Secretary is accountable to no one if the Health National Emergency continues to be extended by Congress every three months.
A significant information operation was set in motion the minute COVID-19 hit. The U.S. government, the intelligence community, the media, and Big Tech colluded to orchestrate and implement an intense pressure campaign designed to get the vaccine legally designated under the Emergency Use Authorization Act while vilifying dissenting doctors, critics, and viable alternative treatments. This designation allowed for speedy manufacturing devoid of the standard safety and public health protocols.
For a vaccine to receive designation under the EUA, there can be no other known treatments or cures. Therefore, many proven treatments such as ivermectin and hydroxychloroquine were blacklisted in the media and dismissed as “horse dewormers” when these cheap, readily available drugs were in the past heralded for their effectiveness.
Eminent COVID-treating doctors such as Peter M. McCullough and Pierre Kory have faced unprecedented attacks on their medical credentials.
Drug insider spills beans: DoD, HHS and Big Pharma committed MASS MURDER with covid "vaccines"
NaturalNews.com / Ethan Huff
(Natural News) Everything from their development to their authorization to their approval to the mandates is a fraud, says pharmaceutical industry insider Sasha Latypova about the so-called “vaccines” for covid.
In a new hour-long presentation – watch it here – Latypova lays out the copious evidence she has compiled – including “receipts” – to show that covid injections are nothing more than a bioweapon that was unleashed on the world by the United States Department of Defense (DoD) via the corrupt U.S. Food and Drug Administration (FDA).
Latypova, who worked with 60 different pharmaceutical companies throughout her 25-year industry career, says that any alleged benefits associated with the shots pales in comparison to the many adverse events they cause, sudden death being one of the most prominent.
It turns out that covid jabs are not pharmaceutical products at all, Latypova found. Instead, they are military bioweapons. (Related: Last year, Latypova’s “Team Enigma” spoke with Dr. Jane Ruby about Donald Trump’s Operation Warp Speed scam and how it was used to unleash these bioweapons.)
While the world has been led to believe that the likes of Pfizer and Moderna are responsible for these deadly shots, the head of the snake looks to be the DoD and other military-industrial complex actors who made them “toxic by design.”
Congress paved way for Operation Warp Speed and the shots’ rapid release nearly 30 years ago
There are various “mechanisms of injury” that were intentionally put into the vial solutions, Latypova explains in the video. Creepily, the mystery concoctions cause the recipient’s body to produce “literally unidentifiable” versions of the SARS-CoV-2 spike protein.
The shots have never been properly tested for safety, either – obviously because they are not safe and were designed to kill. They produce negative efficacy, meaning a person is much better off not getting injected if he or she wants to live.
Basic good manufacturing practices (cGMP) were also not used in the shots’ development, which could explain why some of the vials have been found to contain mystery substances not present in other vials.
Covid jabs were also a long time in the making, it turns out. Latypova uncovered evidence dating back to 1997 when Congress passed two new laws: the FDA Modernization Act and the National Defense Authorization Act (NDAA). Together, these bills allowed for the implementation of “Emergency Use Authorization” (EUA), which is what the FDA used to fast-track the shots onto the market at warp speed.
As Latypova explains, the FDA Modernization Act and the NDAA together “get rid of the FDA’s safety and efficacy regulations and allow the FDA to issue emergency use authorization for certain products which they deem required.”
Originally, there were “pretty strict limitations” on the scope of EUA. Since then, the law has been watered down into oblivion, allowing for just about anything to be forced onto and into people during a declared state of “emergency.”
Changes were also made to 10 U.S. Code § 4021 that amended the Other Transaction Authority (OTA) of the DoD. Here is how Cornell’s Legal Information Institute describes what that accomplished:
“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. 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 short, the changes made to 10 U.S. Code § 4021, implemented by the Obama regime in 2015, allow the DoD to order the production of “undisclosed military prototypes” from private manufacturers like pharmaceutical companies – be sure to watch the full video presentation from Latypova.
Covid jabs are a death sentence for many.
Sources for this article include: