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Zdrowie i gospodarka · 19.11.2012

Medical Devices; Custom Devices; Request for Comments

The Food and Drug Administration Safety and Innovation Act (FDASIA), which was signed into law on July 9, 2012, amended the Federal Food, Drug, and Cosmetic Act (the FD&C Act). The Food and Drug Administration (FDA) is in the process of developing an implementation strategy and policy for the custom device exemption criteria in the FD&C Act amended by FDASIA. FDA is seeking information on appropriate uses of the custom device exemption.

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