Quadrant wins EUA for COVID-19 saliva test

By LabPulse.com staff writers

September 24, 2020 -- Quadrant Biosciences has received emergency use authorization (EUA) from the U.S. Food and Drug Administration (FDA) for its Clarifi COVID-19 test kit.

Developed in partnership with State University of New York (SUNY) Upstate Medical University, the saliva swab test determines the presence or absence of SARS-CoV-2 viral RNA, according to the company. It contains a saliva collection swab and the reagents needed to perform the analysis. Clarifi is available now for clinical laboratories serving patients through physicians' offices, urgent care clinics, and hospitals, Quadrant said.

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Last Updated np 9/29/2020 4:50:55 PM

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