FDA Authorizes Roche's Monkeypox Test
The FDA on Tuesday issued an emergency use authorization to Roche's test for the detection of DNA from monkeypox virus in swab specimens collected from people suspected of the virus infection.
Reuters Health Information
source https://www.medscape.com/viewarticle/984142?src=rss
Reuters Health Information
source https://www.medscape.com/viewarticle/984142?src=rss
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