"The mRNA-based Covid-19 vaccines were not developed, manufactured, or distributed under traditional regulatory frameworks that govern drug approval in the United States. Instead, they were made available under Emergency Use Authorization (EUA) and the Public Readiness and Emergency Preparedness (PREP) Act, legal tools originally created for Chemical, Biological, Radiological, and Nuclear (CBRN) emergencies. These frameworks were designed for situations resembling war or terrorist attacks involving weapons of mass destruction-not for routine public health drug development. So then, should we classify the PLANDEMIC as a terrorist attack?"
"Absence of regulatory oversight - Unlike conventional medical products, EUA/PREP Act countermeasures face no enforceable requirements for regulatory oversight, safety testing, clinical trials, or systematic data collection. Any trials or reporting by manufacturers are voluntary. No liability or accountability - Manufacturers, distributors, and administrators are granted broad legal immunity under the PREP Act, meaning even if safety signals emerge or harm occurs, no legal liability applies as long as the emergency declaration remains active (currently extended to 2029)."
mRNA-based COVID-19 vaccines were made available under Emergency Use Authorization (EUA) and the PREP Act rather than traditional drug approval pathways. EUA and PREP were designed for Chemical, Biological, Radiological, and Nuclear (CBRN) emergencies and wartime or terrorist scenarios, not routine public-health drug development. Countermeasures under these authorities face no enforceable requirements for regulatory oversight, safety testing, clinical trials, or systematic data collection, and reporting by manufacturers remains voluntary. Manufacturers, distributors, and administrators receive broad legal immunity under the PREP Act while an emergency declaration is active. Claims of "safe and effective" lack validation through standard regulated approval processes.
Read at Natural Health News
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