from Daily Clout:
Process 2 was hidden all along in Pfizer’s COVID ‘vaccine’ clinical trial, and the War Room/DailyClout investigators’ findings about it are mind-blowing. The Food and Drug Administration (FDA) knew that the Process 2 subjects had very high levels of adverse events, but there is no evidence that the agency acted on those alarming findings.
This Process 2 ‘trial within a trial’ was not discovered in the tens of thousands of the Pfizer documents released by the FDA until recently. The DailyClout teams were reviewing the expert testimony of Josh Guetzkow Ph.D. of Hebrew University, Tel Aviv, used in a lawsuit in the United Kingdom, and started looking for evidence of the 250 subjects who may have taken part in an experiment on behalf of the European Medicines Agency (EMA).
TRUTH LIVES on at https://sgtreport.tv/
Eagle-eyed War Room/DailyClout volunteer, pharmacist Erika Delph, noted an anomaly in randomization numbers that matched the number and dates of this appended ‘trial within a trial.’ Our data team and medical experts analyzed the data. What they found is shocking: 502 subjects were in a Pfizer COVID vaccine ‘trial within a trial’ and received a drug contaminated with unacceptably high levels of DNA plasmids. It may be tempting to write this off as an accident; however, the documentation notes show that Pfizer knew that it was giving 252 unfortunate trial subjects a completely different injection than that for which they had signed up. This fact alone violates the Nuremberg Code (1947), which states that it is unlawful to run human experiments without full informed consent.
What is Process 2, and why all the fuss?
The terms ‘Process 1’ and ‘Process 2’ were mentioned by Pfizer in the different iterations of the clinical trial protocol for this novel drug platform that would be used worldwide. The ‘process’ refers to the way the ‘vaccine’ was manufactured.
The original manufacturing process of BNT162b2, Pfizer’s COVID ‘vaccine,’ for the clinical trial used a messenger RNA duplication (amplification) technique known as PCR (polymerase chain reaction) — essentially like a photocopier, multiplying/cloning the original mRNA. This is known as ‘Process 1’.
Commercially, this type of process is expensive and would have to be significantly ramped up to provide doses for the whole world. The commercial scaling of the product used a proven way of mass production using e. coli bacteria. This mass production technique is ‘Process 2’. The thorny issue was that ‘Process 2’ used a completely different manufacturing process than that used for the product in the clinical trial (Process 1), and the Emergency Use Authorization (EUA) for the ‘vaccine’ was granted based on Process 1. Moreover, Process 2 was not compliant with Good Manufacturing Practice (GMP). Note the FOIAed national contracts with Pfizer from South Africa and Albania.
Revelations from gene sequencing of the residual product in the vials produced using Process 2 by Kevin McKernan, confirm other groups’ reporting of the determination that there is marked contamination of the modified mRNA with high levels of DNA plasmid fragments.
This contamination is attributed to the use of e-coli during manufacture. These bacteria are naturally found in human gut bacteria and are a regular means of mass-producing mRNA sequences. The required gene is inserted into a ring of DNA, and the bacteria continually replicates these plasmids.
