FDA authorizes new Covid-19 saliva test for emergency use

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FDA authorizes new Covid-19 saliva test for emergency use
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The US FDA has authorized a saliva test for 'emergency use' for diagnosing Covid-19. Rutgers University, where the test was developed in collaboration with other groups, announced the FDA authorization after formally receiving it over the weekend

The US Food and Drug Administration has authorized a saliva test for"emergency use" for diagnosing Covid-19. Rutgers University, where the test was developed in collaboration with other groups, announced the FDA authorization on Tuesday after formally receiving it over the weekend.

Using saliva to diagnose novel coronavirus infections could expand testing capacities across the United States. So far testing for Covid-19 has usually involved nose or throat swabs.

Across the United States, which has faced a shortage of tests, several other laboratories have been working on developing saliva tests and other types of diagnostic testing for Covid-19. So far, during the coronavirus pandemic, the FDA has worked with more than 300 test developers who have said they plan to submit emergency use authorization requests to the agency for their diagnostic tests, the agency announced on Monday.

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