I have 25 years experience as a “Pharmaceutical Clinical Trial Researcher”

I found that Covid-19 products marketed as “vaccines” are not regulated as pharmaceutical medicinal products in US law. Their true legal status is “EUA countermeasures under Public Health Emergency”.

Based on this legal status, despite being described as investigational products and thus can never meet evidentiary standards for safety and efficacy applicable to properly regulated pharmaceuticals.

Absence of enforceable consumer safeguards in relation to these products makes them potential poisons with no lawful mechanisms to rectify the harm while they remain in circulation. 

I investigated the extreme variability of adverse events and deaths lot-to-lot as recorded in VAERS database.  Some lots of the product had only a handful of AEs and others -5/6K and hundreds of deaths. 

Prior to 2020, even a fraction of these events recorded would have stopped any drug product on the market.  The variability was also not random, demonstrating data clustering by geography, date of manufacture and even the alphanumeric codes assigned to the lot numbers.

I later found that covid vaccines are promoted as compliant pharmaceutical products, but they are indeed medical countermeasures that were contracted for by the Department of Defense (DoD) and Biomedical Advanced Research and Development Authority (BARDA). 

As such, they are without any effective regulatory consumer safety oversight at any stage of the process.  This is based on 6 key statutes and related federal laws outlined in the memo we have written for Senator Johnson in December 2022