Zdrowie i gospodarka · 09/09/2022

FDA Revokes Emergency Use Authorizations for COVID-19 Diagnostic Devices

The US Food and Drug Administration (FDA) has revoked two Emergency Use Authorizations (EUAs) for COVID-19 diagnostic devices, issued to Becton Dickinson and Company (BD) and Talis Biomedical Corporation (Talis), due to the lifting of the public health emergency related to the COVID-19 pandemic.