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FDA Greenlights Second Pooled Sample COVID-19 Test As Crucial Tool To Reopen US Economy

US regulators have re-issued an EUA to LabCorp’s COVID-19 molecular diagnostic test for pooled sampling. While the method could speed up testing and use less resources, it also can result in false negatives.

BROOKLYN, NEW YORK - DECEMBER 13, 2019: LABCORP brand logo sign at location entrance

As the US healthcare system struggles with a surge in coronavirus infections and mortality, regulators have given an emergency use authorization (EUA) to a second test that can use pooled sampling to speed up testing and reduce use of testing materials. The manufacturer, however, cautions that patients with negative results may need to get re-tested individually.

A week after the US Food and Drug Administration said it had given temporary market authorization to the first pooled...

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