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You are here: Industry Insights > BioFire RP2.1

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FDA Permits Marketing of First SARS-CoV-2 Diagnostic Test Using Traditional Premarket Review Process americanpharmaceuticalreview
March 24, 2021
The U.S. Food and Drug Administration (FDA) granted marketing authorization of the BioFire Respiratory Panel 2.1 (RP2.1), a diagnostic test for the simultaneous qualitative detection and identification of multiple respiratory viral and ...

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