U.S. Army Staff Sgt. Timmy Underwood, South Carolina National Guard Medical Command medical logistics non-commissioned officer, inspects and stores the first shipment of COVID-19 Moderna vaccinations to arrive at McEntire Joint National Guard Base, South Carolina, Dec. 22, 2020. The South Carolina National Guard is a Moderna Department of Defense (DoD) vaccine pilot program state and is provided a limited DoD allocation for South Carolina National Guard Soldiers and Airmen to have the opportunity to voluntarily take the vaccine. The South Carolina National Guard remains ready to support the counties, local and state agencies and first responders with requested resources for as long as needed in support of COVID-19 response efforts in the state. (U.S. Air National Guard photo by Senior Master Sgt. Edward Snyder, South Carolina National Guard)

FOR IMMEDIATE RELEASE

January 5, 2022

New Docs Reveal Department of Defense Controlled COVID-19 Program from the Start

FDA Vaccine Approval Process was Theater

A combinationofthePREP Act, Emergency Use Authorization, and Other Transactions Authority (OTA) Shielded Big Pharma, Agencies,and Medical Participants that Delivered Unregulated Vaccines from Any Liability

WASHINGTON, DC -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 research and documentswere obtained bya former executive of a pharmaceutical Contract Research Organization (CRO), Sasha Latypova,and intensive legal researcherKatherine Watt.

The Three-Legged Stool

The 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 theU.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

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