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Pathologist Petitions FDA to Halt Pfizer Emergency Use Authorization Until Vaccine Efficacy Confirmed
A recent review of a COVID-19 PCR test, which was signed by 22 international scientists, emphatically stated:
“To determine whether the amplified products are indeed SARS-CoV-2 genes, biomolecular validation of amplified PCR products is essential. For a diagnostic test, this validation is an absolute must. Validation of PCR products should be performed by either running the PCR product in a 1% agarose-EtBr gel together with a size indicator (DNA ruler or DNA ladder) so that the size of the product can be estimated. The size must correspond to the calculated size of the amplification product. But it is even better to sequence the amplification product. The latter will give 100% certainty about the identity of the amplification product. Without molecular validation one cannot be sure about the identity of the amplified PCR products…”
A recent petition to the European Medicines Agency to stay their COVID-19 vaccine trials used similar arguments regarding the inaccuracy of the PCR tests being used and the need for confirmatory sequencing.
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https://childrenshealthdefense.org/defender/fda-petition-halt-pfizer-vaccine-efficacy/?utm_source=salsa&eType=EmailBlastContent&eId=bbd46709-8e18-4db5-800a-5a0279542b94