02/01/2019 12:00 AM EST
Source: World Health Organization (WHO). Published: 2/2019. This four-page document describes the 2019 updated emergency use assessment and listing for Ebola virus disease in vitro diagnostics for STANDARD™ Q Line Ebola Zaire Ag. It is a chromatographic immunoassay for the presumptive qualitative detection of Ebola Zaire virus disease in whole blood, plasma, or serum from individuals with signs and symptoms of Ebola virus infection in affected areas in conjunction with relevant epidemiological risk factors. (PDF)
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