Business · 09/01/2017

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 the Zika virus, in response to the ongoing outbreak in the Americas, following a determination by the Secretary of Health and Human Services (HHS) on February 26, 2016.