Business · 03/11/2016
FDA Issues Emergency Use Authorizations for Zika Virus Detection Devices
The US Food and Drug Administration (FDA) has granted two Emergency Use Authorizations (EUAs) for in vitro diagnostic devices to detect the Zika virus, following a public health emergency determination by the Secretary of Health and Human Services in February 2016.
Original source language: Federal Register — Food and Drug AdministrationOpen original release →