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Business · 23/07/2001

FDA Announces Approval of Adverse Event Pilot Program for Medical Devices

The FDA has announced that it has received approval from the Office of Management and Budget (OMB) to collect information on its Adverse Event Pilot Program for Medical Devices, as required by the Paperwork Reduction Act of 1995.

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

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