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Covid mRNA Impfstoffe wurden unter militärischem Protokoll entwickelt und erforderten keine Sicherheitsüberwachung
The claims made in this article are based on an analysis of the contractual and regulatory framework applied by the U.S. Government to the development, manufacture, and acquisition of the Covid mRNA vaccines. The author specifically uses the BioNTech/Pfizer agreements as an example to illustrate their points. The analysis suggests that the vaccines were acquired and authorized through mechanisms designed to rush medical countermeasures to the military during emergencies involving weapons of mass destruction. These mechanisms did not require adherence to any laws or regulations related to vaccine development or manufacturing. The FDA’s Emergency Use Authorization for the vaccines was based on clinical trials and manufacturing processes conducted with no binding legal standards, safety oversight, or regulation. The author argues that the assertion of the vaccines being „safe and effective“ was based on aspirations, opinions, beliefs, and presumptions of government employees
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Covid mRNA Vaccines Were Developed Under a Military Protocol and Required No Safety Oversight
When everyone from the President to your primary care doctor declared loudly and wholeheartedly in December 2020 that the newly FDA-authorised Covid mRNA vaccines were ‘safe and effective’ – what were those claims based on? In this article, I will review the contractual and regulatory framework applied by the U.S. Government to the initial development, manufacture and acquisition of the Covid mRNA shots. I will use the BioNTech/Pfizer agreements to illustrate the process. The analysis will show that: The Covid mRNA vaccines were acquired and authorised through mechanisms designed to rush medical countermeasures to the military during emergencies involving weapons of mass destruction. These mechanisms did not require the application of, or adherence to, any laws or regulations related to
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