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Zdrowie i gospodarka · 05/10/2020

FDA Revokes Emergency Use Authorizations for COVID-19 Tests

The US Food and Drug Administration (FDA) has revoked the emergency use authorizations for two COVID-19 tests, including one developed by Autobio Diagnostics Co. Ltd. and another for in vitro diagnostic SARS-CoV-2 antibody tests, due to concerns over their accuracy and effectiveness.

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