The FDA Granted Emergency Use Authorization To Labcorp's Mpox PCR Test Home Collection Kit To Diagnose Infection With Non-Variola Orthopoxvirus, As The First Mpox At-home Collection Kit Authorized By FDA
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The FDA has granted Emergency Use Authorization to Labcorp's Mpox PCR Test Home Collection Kit, marking it as the first Mpox at-home collection kit to receive such authorization. This kit is designed to diagnose infection with non-variola orthopoxvirus.
April 10, 2024 | 10:52 am
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Labcorp's Mpox PCR Test Home Collection Kit has received Emergency Use Authorization from the FDA, making it the first at-home collection kit for Mpox diagnosis.
The FDA's Emergency Use Authorization of Labcorp's Mpox PCR Test Home Collection Kit is a significant regulatory milestone for the company. This authorization not only enhances Labcorp's product portfolio but also positions the company as a leader in the diagnostic space for emerging health threats. The news is likely to be viewed positively by investors, potentially leading to a short-term uptick in Labcorp's stock price due to increased investor confidence in the company's innovation capabilities and market position.
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