Novel coronavirus: FDA issues Emergency Use Authorization for the first diagnostic test
by Press Release from Outbreak News Today on (#4YXGF)
The U.S. Food and Drug Administration issued an emergency use authorization (EUA) today to enable emergency use of the Centers for Disease Control and Prevention's (CDC) 2019-nCoV Real-Time RT-PCR Diagnostic Panel. To date, this test has been limited to use at CDC laboratories; today's authorization allows the use of the test at any CDC-qualified lab ["]
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