Discussion about Regulatory and Scientific Fraud in Pfizer Preclinical Studies

A conversation with my colleague Hedley Rees regarding Pfizer preclinical studies that were recently released by FIOA lawsuit. This is the stuff Pfizer and FDA were trying to keep secret for 75 years! We learned why - many violations of standard safety evaluations, disregard for major parts of safety studies such as Safety Pharmacology (i.e. effects in major organ systems such as cardiovascular, liver, kidney, blood and other organ systems) entirely omitted because Pfizer claimed those requirements did not apply to this completely novel technology! More evidence of fraud and regulatory collusion.

Correction: there are 2 versions of the product, V8 and V9 mentioned in the package of documents. Pfizer states that V9 is the final vaccine candidate. Specifically that it is BNT162b2 (V9). I am still investigating the issue of multiple versions of products being included in various stages of development. For example, I already found that in the Phase I/II human clinical trial Pfizer used BNT162b1 (not BNT162b2 as they claim being final vaccine candidate). This is extremely concerning and not allowed practice under the same IND (Investigational New Drug) application.