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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Cepheid Receives Emergency Use Authorization For SARS-CoV-2, Flu A, Flu B, and RSV Combination Test
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Xpert® Xpress SARS-CoV-2 - FDA Emergency Use Authorization
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FDA grants EUA to Cepheid's rapid Covid-19/Flu/RSV diagnostic test
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Diagnostic accuracy of the Cepheid Xpert Xpress and the Abbott ID NOW assay for rapid detection of SARS‐CoV‐2: A systematic review and meta‐analysis - Lee - 2021 - Journal of Medical Virology
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FDA authorized molecular point-of-care SARS-CoV-2 tests: A critical review on principles, systems and clinical performances - ScienceDirect
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Diagnostics, Free Full-Text
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Multicenter Evaluation of the Cepheid Xpert Xpress SARS-CoV-2 Test
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FDA approves new coronavirus test that can have 'results within hours' instead of days
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Four-In-One-Test for Respiratory Virus Season
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Coronavirus COVID-19