Department of Defense Documents Reveal No COVID-19 Vaccine Clinical and Manufacturing Standards of Practice
Question to Congress: What have millions of Americans injected on your watch?
FOR IMMEDIATE RELEASE
January, 2022
Department of Defense Documents Reveal No COVID-19 Vaccine Clinical and Manufacturing Standards of Practice
DOCS Reveal No COVID Clinical and Manufacturing Standards of Practice
Question to Congress: What have millions of Americans injected on your watch?
WASHINGTON, DC - Newly released documents from the Department of Defense (DOD) reveal that no clinical and manufacturing standards of practice have been applied to the COVID-19 vaccination program. The U.S. Department of Health and Human Services (HHS) along with the DOD originally and continue to contract with large pharmaceutical companies such as Pfizer to produce “prototypes” for COVID-19 shots.
Pfizer is among DOD’s largest contractors. In December 2020, the U.S. Army awarded an estimated $10 billion contract to Pfizer for 500 million replicas of the COVID-19 shot at $20 per dose. In 2022, the U.S. Army paid Pfizer an estimated $4.8 billion modification contract to supply Paxlovid COVID-19 treatment pills to the U.S. Army’s Contracting Command in Maryland.
The contracts were released by FOIA and analyzed by Sasha Latypova a highly regarded former executive of a pharmaceutical Contract Research Organization (CRO) and intensive legal researcher Katherine Watt. Throughout her career, pharmaceutical companies including Pfizer have contracted with Latypova more than sixty times.
In addition, the documents provide evidence that the content of what Americans believe to be the COVID19 vaccine is unknown and unregulated outside of the pharmaceutical companies.
For example:
mRNA in the shots has never been fully described, no manufacturer ever provided evidence that the expressed spike protein is the "correct" protein (in fact we know it is not correct because it is heavier than Wuhan spike by molecular weight). Pfizer submitted fake computer-generated images of these tests, and even those fakes were not everything that needed to be submitted, they never provided sequencing results.
The proprietary lipids ALC-0315 and ALC-0159 are completely novel, proprietary, and not described anywhere. They are not pharmaceutical grade and not labeled for human use.
No tests for conformity to the label at the vial or dose level exist. No manufacturer tests that for example, there is really 225 mcg of mRNA BNT162b2 in the vial, and that this mRNA conforms to the specification (i.e. it has a length of 4824 nucleotides and specific letter sequence). That's not done anywhere. Forget about at the individual dose level since they are manually made by God knows who in what conditions in a parking lot.
While independent vial testing is prohibited, nonetheless, direct vial testing by at least 26 research teams in 16 countries has shown that there is often no mRNA, that there are gigantic amounts of impurities (both genetic and chemical, like toxic metals), there are big particles, inclusions, all sorts of junk floating around, and does not correspond to the labels at all.
Perhaps the biggest shock is the fact that the program is not controlled by the FDA or any public health agency, but rather the National Security Council. As it turns out, Operation Warp Speed never actually slowed down. Pfizer among the biggest contractors to the Department of Defense.
In fact, what Congress and the administration have been hiding is the fact that the vaccine is not a traditional vaccine at all, but rather considered a “countermeasure” to a foreign attack. And because the director of Health and Human Services declared the vaccine a countermeasure under the Emergency Use Authorization, these countermeasures are disallowed to be tested or investigated.
In other words, all the participants in the FDA trials, investigators and many FDA staff were duped, treated as actors participating in a predetermined process.
A combination of the PREP Act, Emergency Use Authorization (EUA), and Other Transactions Authority (OTA) Shielded Big Pharma, Agencies, and Medical Participants that Delivered Unregulated Vaccines from Any Liability
“We need Congress to act - they may not be able to revoke the damage done from the of bio-agents unknowingly injected into hundreds of millions of Americans, but they can be damn sure not to let it happen again and from here on out maintain transparence in any type of “pandemic” scenario.
The Department of Defense mislead the public about the legal status and the scope of the prototypes that they ordered from the pharmaceutical companies and other defense contractors. DOD ordered only large-scale manufacturing demonstrations. Further, as prototypes used under Emergency Use Authorization during PHE, Covid Countermeasures NEED NOT to comply with the US laws for manufacturing, safety, and labeling (21 USC 360bbb-(k)). The US Government and DOD authorized and funded the deployment of non-compliant chemical and biological materials (also a designated class of biowarfare agents) without clearly communicating their "demonstration" and "prototype" legal status, not making these materials subject to normal regulatory oversight, all while maintaining a fraudulent pseudo - "regulatory" presentation to the public.
The Four-Legged Stool
The undercover operation was orchestrated utilizing four critical legal maneuvers:
1. Public Health Emergency (PHE),
2. Emergency Use Authorization (EUA),
3. Public Readiness and Emergency Preparedness (PREP Act),
4. Other Transactions Authority (OTA)
On January 31, 2020, Health and Human Services (HHS) Secretary, Alex M. Azar declared a Public Health Emergency (PHE) pursuant to section 319 of the Public Health Services (PHS) Act, 42 U.S.C. 247d, for the entire United States. A PHE bestows a substantial amount of war-time authority upon the HHS Secretary. This PHE declaration was one day after a similar declaration by the WHO.
On March 10, 2020, HHS Secretary, Alex M. Azar, issued a “Notice of Declaration” to activate the PREP Act to provide liability immunity for Covered Persons and Covered Countermeasures. The PREP Act declaration filled six pages of the Federal Register on March 17, 2020 that can be found here, https://www.govinfo.gov/content/pkg/FR-2020-03-17/pdf/2020-05484.pdf
Covered Countermeasures are any antiviral, any other drug, any biologic, any diagnostic, any other device, or any vaccine, used to treat, diagnose, cure, prevent, or mitigate COVID–19. The administration of President Trump placed 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. According to government documents acquired by Latypova, $47.5 Billion was awarded in contracts by BARDA as of 10/29/2021 for Covid-19 vaccines, therapeutics and diagnostics.
"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 (OTA). 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.
Here is a typical contract scope for “vaccines”:
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