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Zdrowie i gospodarka · 26/11/2024

FDA Releases Guidance on Ethylene Oxide Sterilization Facility Changes for Class III Devices

The Food and Drug Administration (FDA) has released a final guidance document to help manufacturers of Class III devices affected by potential disruptions in ethylene oxide sterilization facilities, providing recommendations for enforcement discretion in the implementation of sterilization site changes.

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