Latest news from Clinical Reference Laboratory on Newswise en-us Copyright 2024 Newswise 115 31 / /images/newswise-logo-rss.gif /articles/clinical-reference-laboratory-receives-fda-emergency-use-authorization-for-best-in-class-self-collected-covid-19-saliva-test/?sc=rsin /articles/clinical-reference-laboratory-receives-fda-emergency-use-authorization-for-best-in-class-self-collected-covid-19-saliva-test/?sc=rsin Fri, 31 Jul 2020 09:00:03 EST Today, Clinical Reference Laboratory (CRL), one of the largest privately held clinical testing laboratories in the U.S., announced that it received FDA Emergency Use Authorization (EUA) and is scaling up capacity for CRL Rapid Response(tm), a saliva-based COVID-19 RT-PCR test that can be self-collected at home, work or any other setting. Clinical Reference Laboratory