Sunnyvale, CA-based Cepheid received Emergency Use Authorization from the U.S. Food & Drug Administration (FDA) for Xpert Xpress SARS-CoV-2, a rapid molecular diagnostic test for qualitative detection of SARS-CoV-2, the virus causing COVID-19. Cepheid’s test is reportedly the first test approved for coronavirus that can be done bedside and get results in less than an hour. Previously…
Emergency Approval Granted for Cepheid’s Rapid Results COVID-19 Test
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