VIVO - Meridian Bioscience gets FDA EUA for Revogene SARS-CoV-2 molecular assay
Meridian Bioscience (NASDAQ:VIVO) announces that their Revogene SARS-CoV-2 assay was granted Emergency Use Authorization (EUA) by the U.S. FDA. Shares jump more than 7% premarket. The Revogene SARS-CoV-2 assay is a molecular diagnostic test for the qualitative detection of the SARS-CoV-2 virus, the causative agent of COVID-19. Meridian expects to begin shipping the product before the end of its fiscal first quarter, ending December 31, 2021.
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Meridian Bioscience gets FDA EUA for Revogene SARS-CoV-2 molecular assay