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Zdrowie i gospodarka · 04/08/2009

FDA Issues Emergency Use Authorizations for In Vitro Diagnostic Devices

The Food and Drug Administration (FDA) is issuing two Emergency Use Authorizations (EUAs) for certain in vitro diagnostic devices, following a public health emergency declaration due to the Swine Influenza A outbreak, which affects national security. The EUAs contain conditions for the emergency use of authorized in vitro diagnostics.

Source: Federal Register — Food and Drug AdministrationOpen original release →