FDA Authorizes Additional OTC Home Test to Increase Access to Rapid Testing for Consumers
The following is attributed to Jeff Shuren, M.D., J.D., director of FDA’s Center for Devices and Radiological Health Today, the U.S. Food and Drug Administration issued an emergency use authorization (EUA) for the ACON Laboratories Flowflex COVID-19 Home Test, an over-the-counter (OTC) COVID-19 antigen test, which adds to the growing list of tests that can be … Continue reading FDA Authorizes Additional OTC Home Test to Increase Access to Rapid Testing for Consumers
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