Zdrowie i gospodarka · 19/09/2019

FDA Revokes Authorization for Zika Virus Diagnostic Test

The US Food and Drug Administration (FDA) has revoked the Emergency Use Authorization (EUA) for Luminex Corp.'s xMAP MultiFLEX Zika RNA Assay, a diagnostic test for Zika virus, due to a request from the company itself, citing the Federal Food, Drug, and Cosmetic Act (FD&C Act).