Today we discuss "adulteration" of the COVID vaccine. Basically, it is contamination that is not otherwise disclosed. If the contamination exceeds allowed specifications, and the packaging does not disclose (i.e., consumer not aware), then it meets the criteria for "adulteration." So if that happens, there is a process the FDA has set, such that they issue a requirement that the manufacturer places a hold on the product. It then could lead to the vaccination being withdrawn from the market. In our guest's opinion, such criteria has been met for adulteration. If its proved that Pfizer, Moderna, and AstraZeneca are guilty of this, then there is a possibility of DNA migration, and these companies are liable.
In this recent COVID case, we do know that processes were bypassed and the vaccine was sent to market. If the contamination did get into the vaccine, a question arises, as to whether it was accidental or intentional. Our guest is familiar with circular DNA plasmas produced by bacteria as a source of DNA to make the RNA. Then to get rid of the DNA, you use enzymes. That part appears to have not been well developed as a process.
It appears that a rushed switch took place. FDA did not force them to do the work as it was jammed through under the assumption that we would have a national crisis. A 3.4% mortality rate (sound familiar?) was used in event 201 war game planning in fall of 2019. This was needed when the insiders became aware that there was some kind of escape of a virus. The WHO took the 3.4% number to be fact - but it was based on modelling, not measured data. This gives you a flavor of our discussion today. Participants: Dr. Robert Malone, Dan Elmendorf