Business · 17/04/2014

FDA Authorizes Emergency Use of Influenza A (H7N9) Diagnostic Device

The US Food and Drug Administration (FDA) has issued an Emergency Use Authorization (EUA) for an in vitro diagnostic device to detect the novel influenza A (H7N9) virus, which was detected in China in 2013, following a public health emergency determination by the Secretary of Health and Human Services (HHS) on April 19, 2013.