FDA issued Emergency Use Authorization to Thermo Fisher Scientific for diagnostic test for COVID-19

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On Mar. 13, 2020, Thermo Fisher Scientific announced the FDA has issued an emergency use authorization (EUA) for its diagnostic test that can be used immediately by CLIA high-complexity laboratories in the U.S. to detect nucleic acid from SARS-CoV-2, the virus that causes COVID-19, and not for any other viruses or pathogens.

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Source: Thermo Fisher Scientific
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