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FDA authorizes Quest Diagnostics' proprietary monkeypox test

Quest Diagnostics, a leading provider of diagnostic information services, has announced that it has received emergency use authorization (EUA) from the U.S. Food and Drug Administration (FDA) for the company's lab-developed molecular diagnostic test to aid in the diagnosis of infection with the Monkeypox virus. 
United States Jayg Wohlgemuth Centers For Disease Human Services Drug Administration York Department Of Health

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