Zdrowie i gospodarka · 28/10/2016

FDA Issues Emergency Use Authorizations for Zika Virus Diagnostic Devices

The US Food and Drug Administration (FDA) has granted four emergency use authorizations for in vitro diagnostic devices to detect and/or diagnose Zika virus, in response to the ongoing outbreak in the Americas, following a public health emergency determination by the Secretary of Health and Human Services on February 26, 2016.