Zdrowie i gospodarka · 05/07/2024

FDA Authorizes Emergency Use of In Vitro Diagnostic Device for Mpox

The FDA has issued an Emergency Use Authorization for an in vitro diagnostic device to detect Mpox, following a public health emergency declaration by the Secretary of HHS in response to the Mpox outbreak.

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

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Zdrowie i gospodarka · 10/5/2026

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