A new analysis on the creation of the mRNA shots that were purported to help victims fight the COVID-19 virus that came out of a Chinese research lab and killed millions worldwide shows that they were imposed on Americans by bypassing all of the "Laws or regulations that we count on to protect use from potentially harmful, or deadly, medical products".
The analysis by Debbie Lerman, a graduate of Harvard who is a retired science writer, charged in the article that: "The COVID-19 mRNA vaccines were acquired and authorized through mechanisms designed to rush medical countermeasures to the military during emergencies involving weapons of mass destruction."
Secondly, she said, "These mechanisms did not require the application of, or adherence to, any laws or regulations related to vaccine development or manufacturing."
"What all of this means is that none of the laws or regulations that we count on to protect us from potentially harmful, or deadly, medical products was applied to the COVID-19 mRNA vaccines," she charged.
The specific OTA for Pfizer, the analysis confirms, was set up to have the government pay Pfizer "To show that it can manufacture 100 million doses of a never-before produced or tested product, while also acquiring those 100 million doses, and potentially hundreds of millions more."
As for regulatory oversight of the development and manufacturing processes, the analysis revealed, "Pfizer will meet the necessary FDA requirements for conducting ongoing and planned clinical trials, and with its collaboration partner, BioNTech, will seek FDA approval or authorization for the vaccine, assuming the clinical data supports such application for approval or authorization."
The analysis pointed out: "Here's the kicker about EUA: because it was intended to be issued only in war and WMD-related emergencies, there are no legal requirements for how it is issued, beyond the determination of the FDA that such authorization is appropriate. There are no legal standards for how clinical trials are conducted. There are no laws regulating the manufacturing processes. There are only 'reasonable beliefs' based on whatever evidence is available to the FDA at the time that it makes its determination."
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