Yesterday the U.S. health regulator 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.
https://www.pharmalive.com/wp-content/uploads/2021/10/Roche-launches-genomic-profiling-kit-to-ease-cancer-research-Reuters-10-25-21.jpeg171295Reuters Healthhttps://www.pharmalive.com/wp-content/uploads/2020/01/Pharmalive_4c-300x37.pngReuters Health2022-11-15 16:36:352022-11-16 09:10:17U.S. FDA authorizes Roche’s monkeypox test
