Zdrowie i gospodarka · 17/11/2017

FDA Releases Draft Guidance on Evaluation of Devices Used with Regenerative Medicine Advanced Therapies

The US Food and Drug Administration (FDA) has made available a draft document outlining its approach to evaluating devices used in regenerative medicine therapies, with the goal of simplifying and streamlining regulatory requirements for device manufacturers and developers.

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

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