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Zdrowie i gospodarka · 02/06/2020

FDA Announces Process for Publishing Emergency Use Authorizations for COVID-19 Medical Devices

The Food and Drug Administration (FDA) has outlined a plan to quickly publish Emergency Use Authorizations (EUAs) for medical devices related to COVID-19, aiming to facilitate rapid response to the public health emergency.

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