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Biomarker, Innovation

US FDA re-authorises EUA for Meridian’s Revogene SARS-CoV-2 test

August 1, 2022

Via: medicaldevice-network.com

The US Food and Drug Administration (FDA) has re-authorised the emergency use authorization (EUA) for Meridian Bioscience’s Revogene SARS-CoV-2 molecular assay. The regulator initially granted EUA for the Covid-19 molecular diagnostic test last November. However, the company decided to delay […]

Tag: molecular diagnostic test

US FDA re-authorises EUA for Meridian’s Revogene SARS-CoV-2 test

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Tag: molecular diagnostic test

US FDA re-authorises EUA for Meridian’s Revogene SARS-CoV-2 test

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