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Sasha Latypova, who is an expert in drug development, explains | Children's Health Defense Europe

Sasha Latypova, who is an expert in drug development, explains how the manufacturers of the COVID mRNA vaccines, Pfizer and Moderna, skipped essential preclinical safety studies, and how the FDA let them get away with it, failing in its duty to protect the public from these unsafe medicines.

The FDA remains dysfunctional as of today, and it cannot be trusted with protecting the public from harm caused by any future vaccines or other medicines.

Watch the full presentation here: https://rumble.com/v18fkf9-pfizers-and-modernas-preclinical-vaccine-trials-evidence-of-scientific-and-.html