By Capt Joseph R. John, September 20, 2021: Op Ed #564
The Federal Drug Administration (FDA) has a division that specializes in vaccines, the Office of Vaccine Research and Review (OVRR). It has always been up to the OVRR to give the final approval for a vaccine after specific testing. The procedures to green light one of the three Test Inoculations that were operating under the Special Emergency-Use Provision were violated by passing the FDA’s own regulations. The FDA Vaccine Advisory Panel should have been allowed the time to analyze the tests and given the authority for final approval for the booster inoculation for the Delta Variant, being demanded by Anthony Fauci at the NIH, and being eyed by big pharma-despots hungry for billions in more profits.
The FDA’s bureaucratic culture and many-decades-old penchant for testing and keeping drugs in the approval process…
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