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Quest Diagnostics Incorporated (via Public) / FDA Authorizes Quest Diagnostics Proprietary Monkeypox Test for Emergency Use

Quest Diagnostics Incorporated (via Public) / FDA Authorizes Quest Diagnostics Proprietary Monkeypox Test for Emergency Use
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FDA Authorizes Quest Diagnostics Proprietary Monkeypox Test for Emergency Use

Quest monkeypox test receives FDA emergency use authorization

On Sept. 7, Quest Diagnostics announced its monkeypox test received emergency use authorization from the FDA for use by authorized labs. 

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. 

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