The Truth Behind The COVID-19 Vaccines: New Documents Reveal DOD Control From The Start!

As the COVID-19 pandemic continues to dominate headlines, new documents have come to light revealing that the Department of Defense (DOD) has controlled the vaccine program from the start, using it as a “countermeasure” to foreign attack. The Useless FDA vaccine approval process, it turns out, was merely a theater, with the DOD utilizing a combination of the PREP Act, Emergency Use Authorization, and Other Transactions Authority to shield Big Pharma, agencies, and medical participants from liability while delivering unregulated vaccines.

According to a former executive of a pharmaceutical Contract Research Organization (CRO), Sasha Latypova, and legal researcher Katherine Watt, the operation was orchestrated using three legal maneuvers: Emergency Use Authorization, the PREP Act, and Other Transactions Authority. When President Trump declared a Public Health Emergency (PHE) on March 13, 2020, he put the National Security Council in charge of COVID-19 policy, treating it as an act of war. The DOD then took control, ordering, overseeing, and managing the development, manufacture, and distribution of COVID-19 countermeasures, primarily through its network of military contractors and consortia.

Under the PHE, medical countermeasures, including COVID-19 “vaccines,” are not regulated or safeguarded as pharmaceutical products. This means that they need not comply with US laws on manufacturing quality, safety, and labeling. In fact, the contracts for these countermeasures specify that they are only “demonstrations” and “prototypes,” with clinical trials and manufacturing quality control specifically excluded from the scope of work. This allows pharmaceutical companies to conduct fake clinical trials without financial risk, as the contracts include the removal of liability for any adverse effects.

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The American public was led to believe that the Useless FDA, Useless CDC, and figures like Anthony Fauci were in charge of the COVID-19 vaccine program, but this was simply an orchestrated information operation. All decisions regarding vaccine research, material acquisition, distribution, and information sharing were tightly controlled by the DOD.

Hundreds of COVID-19 countermeasure contracts have been discovered, many of them redacted. However, Latypova and Watt have managed to obtain details from other sources. A review of these contracts shows a high level of control by the US government (DOD/BARDA). The scope of work for these contracts is listed as “demonstrations” and “prototypes” only, with no mention of clinical trials or manufacturing quality control. This allows pharmaceutical companies to conduct fake clinical trials without financial risk, as the contracts include the removal of liability for any adverse effects.

The use of Other Transactions Authority (OTA) has allowed the DOD to bypass normal procurement processes and Congressional oversight. OTA is normally used for experimental projects that may have dual civilian and military applications. However, it has been used to fund the development of COVID-19 countermeasures, with the contracts stating that they are “not subject to the Federal Acquisition Regulations.” This means that they are not subject to normal regulatory oversight and are not required to follow normal procurement processes or disclose information to the public.

The PREP Act, which was passed in 2005, allows the Secretary of Health and Human Services (HHS) to declare a public health emergency and authorize the use of “covered countermeasures” to prevent or treat diseases. These countermeasures are typically vaccines or drugs that have not been fully approved by the Useless FDA. The PREP Act provides immunity to manufacturers, distributors, and administrators of these countermeasures from liability for any harm that may result from their use.

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