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Monkeypox Assay Granted Emergency Use Authorization

Thermo Fisher Scientific’s Applied Biosystems TaqPath Monkeypox/Orthopox Virus DNA Kit, a polymerase chain reaction (PCR) test designed to detect non-variola Orthopoxviruses, including monkeypox virus, in approximately three-and-a-half hours, has been granted Emergency Use Authorization (EUA) by the US Food and Drug Administration (FDA). Click to read more.

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FDA Grants Emergency Use Authorization for Thermo Fisher Scientific s Monkeypox Test

FDA Grants Emergency Use Authorization for Thermo Fisher Scientific s Monkeypox Test
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