Hill February 24, 2023
Jared Gans

The Food and Drug Administration (FDA) approved the first over-the-counter at-home test for both COVID-19 and the flu on Friday.

The FDA said in a release that the test can differentiate between and detect Influenza A and B, which most commonly cause the flu in humans, and SARS-CoV-2, the virus that causes COVID-19.

Jeff Shuren, the director of the FDA’s Center for Devices and Radiological Health, said in the release that the test is a “major milestone” to increase consumers’ access to tests that can be taken at home.

“The FDA strongly supports innovation in test development, and we are eager to continue advancing greater access to at-home infectious disease testing to best support public health needs,”...

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Topics: FDA, Govt Agencies, Healthcare System, Home, Patient / Consumer, Provider, Public Health / COVID
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