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The FDA is now classifying LDTs as medical devices. This follows criticism following the FDA not approving COVID-19 rapid tests more quickly in 2020.
(CTN News) - In a final rule published on Monday by the US Food and Drug Administration (FDA), the agency seeks to ensure the safety................
Two senior FDA officials, including Dr. Robert Califf, the agency head, recently published a journal article entitled "Is Vaccination Approaching a Dangerous Tipping Point?" They make a compelling case that we are facing a crisis:
Observers expect the move will face legal challenges, prompt intervention from Congress.
View the The Bedford Gazette for Tuesday, April 30, 2024