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FDA Approves New Rapid Coronavirus Test That Can Give Results In 45 Minutes

22 Mar 2020

The U. S. Food and Drug Administration (FDA) has granted emergency use authorization (EUA) to Cepheid for their Xpert® Xpress SARS-CoV-2 test.

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This content was originally published by Forbes Magazine. Original publishers retain all rights. It appears here for a limited time before automated archiving. By Forbes Magazine

Covid-19 – Johns Hopkins University

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