Xpert® Xpress SARS-CoV-2 - FDA Emergency Use Authorization
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Xpert® Xpress SARS-CoV-2/Flu/RSV received Emergency Use Authorization from the US FDA to support the global fight against COVID-19, with rapid detection of the current coronavirus SARS-CoV-2.
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Xpert® Xpress SARS-CoV-2 - FDA Emergency Use Authorization
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Cepheid Receives Emergency Use Authorization For SARS-CoV-2, Flu A, Flu B, and RSV Combination Test
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Cepheid gets FDA nod for EUA 45-minute coronavirus test, 2020-03-23
Cepheid Receives Emergency Use Authorization from FDA for Rapid SARS-CoV-2 Test - Mar 21, 2020
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Cepheid Receives Emergency Use Authorization from FDA for Rapid SARS-CoV-2 Test - COVID-19 - mobile.
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Xpert® Xpress SARS-CoV-2 - FDA Emergency Use Authorization
Cepheid on LinkedIn: Cepheid Receives Emergency Use Authorization from FDA for Rapid SARS-CoV-2…
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Cepheid Receives Emergency Use Authorization for Xpert® Xpress CoV-2 plus
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Cepheid receives EUA from FDA for SARS-CoV-2 Test
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Diagnostics, Free Full-Text
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Utility of SARS-CoV-2 rapid antigen testing for patient triage in the emergency department: A clinical implementation study in Melbourne, Australia - The Lancet Regional Health – Western Pacific
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Design and Implementation of Improved SARS-CoV-2 Diagnostic Assays To Mitigate the Impact of Genomic Mutations on Target Failure: the Xpert Xpress SARS-CoV-2 Experience
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CRISPR–Cas12-based detection of SARS-CoV-2