FDA opens door to rapid, at-home testing for COVID-19

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FDA opens door to rapid, at-home testing for COVID-19
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At-home testing could transform the fight against the novel coronavirus.

Several testing experts, including, said the FDA's move is a step in the right direction and could encourage companies to pursue inexpensive, rapid, at-home tests.

The template also outlines how accurate the tests must be, with slightly lower standards than lab-based tests. Similar rapid tests used to diagnose strep throat miss as many as one in five people who are infected, so physicians normally send a throat culture to a lab to confirm the diagnosis, said Dr. Emily Volk, president-elect of the College of American Pathologists. Such confirmatory testing usually takes several days.

Another $50 million is available to scale up manufacturing and could be distributed to any contestant during the competition, said Jeff Huber, president and co-founder of OpenCovidScreen, whose company is launching the competition in collaboration with XPRIZE.

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