Ebola -- Guinea
22 Apr 2016: Authorization of emergency use of an in vitro diagnostic device for detection of Ebola Zaire virus; availability
[The Food and Drug Administration (FDA) is announcing the issuance of an Emergency Use Authorization (EUA) (the Authorization) for an in-vitro diagnostic device for detection of the Ebola Zaire virus in response to the Ebola virus outbreak in West Africa. The FDA issued this Authorization under the Federal Food, Drug, and Cosmetic Act (the FD&C Act), as requested by
Read more about it at HealthMap Global Disease Alerts via http://bit.ly/1NUZp9r
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