FDA authorizes rapid COVID 19 antigen test

Illustration by Alex Castro / The Verge

The Food and Drug Administration has granted the first emergency use authorization to diagnostic healthcare company Quidel Corp. for the first COVID-19 antigen test, the agency announced. Antigen tests can quickly detect the coronavirus, but are generally considered less accurate than other types of tests that search out the virus.

Antigen tests for COVID-19 are akin to rapid flu or strep tests. This test can be run in a lab or in a doctor’s office, and only takes about 15 minutes.

The tests typically used to diagnose COVID-19, called PCR tests, search out the genetic sequence of the coronavirus in a swab collected from a patient’s nose or throat. Antigen tests, on the other hand, look for molecules on the surface of the virus. They…

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via The Verge – All Posts

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