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March 23, 2020

Portfolio News: US FDA grants EUA for Cepheid’s SARS-CoV-2 test

Band HQ
March 23, 2020
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Cepheid has received emergency use authorization (EUA) from the US Food and Drug Administration (FDA) for its rapid molecular diagnostic test, Xpert Xpress SARS-CoV-2. The test is designed for the qualitative detection of SARS-CoV-2 virus, which causes coronavirus (Covid-19) disease.

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