There has been a leak of European Medicine Agency (EMA) emails and other Pfizer-related confidential reports, prior to the authorization of the Pfizer-BioNTech Covid-19 vaccine. As stated below, “By late November 2020, regulators including, US FDA, European Medicines Agency, Health Canada and the UK’s MHRA, were all aware of the significant loss of RNA integrity of the commercial batches (~55% mRNA integrity) of the Pfizer-BioNTech vaccine compared to the clinical ones (~78% mRNA integrity). This was classified by EMA as a “major objection” along with observed visible particles, which were classified as “impurities.”
A leaked 26 November PowerPoint presentation of a meeting between Pfizer-BioNTech and the EMA revealed how this major objection was shockingly ‘resolved’- the RNA integrity specification was simply lowered to 50%, therefore half of all mRNA molecules in the commercial batches were allowed to be truncated (not intact).” In short, as in the US and all other jurisdictions, the authorities did not do due diligence, as would be expected with other vaccines, and allowed al that we now see to unfold.