Business · 22/04/2016

FDA Authorizes Emergency Use of In Vitro Diagnostic Device for Zika Virus Detection

The US Food and Drug Administration (FDA) has issued an Emergency Use Authorization (EUA) for an in vitro diagnostic device to detect Zika virus, in response to the ongoing Zika virus outbreak in the Americas, following a determination by the Department of Health and Human Services (HHS) Secretary on February 26, 2016.