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Business · 25/02/1998

FDA Publishes Guidance Documents for Medical Device Industry Implementation of FDAMA

The Food and Drug Administration (FDA) has released six guidance documents outlining the Center for Devices and Radiological Health's approach to implementing relevant sections of the Food and Drug Administration Modernization Act of 1997 (FDAMA), with public comments invited on the documents.

Original source language: Federal Register — Food and Drug AdministrationOpen original release →

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