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FDA Eager To Authorize More Rapid Antigen COVID-19 Tests

The US FDA’s diagnostics chief says the agency isn’t seeing many submissions for rapid antigen tests, but is eager to authorize them. 

Coronavirus

While the US Food and Drug Administration has given emergency use authorization (EUA) to a slew of COVID-19 diagnostics tests, the agency hasn’t seen as many applications for rapid antigen tests, which could be a game-changer in getting Americans back to work and school.

Tim Stenzel, director of the FDA’s Office of In Vitro Diagnostics and Radiological Health (OIR), said while to date the agency has authorized 243 tests to diagnose COVID-19, only four...

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