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Business · 14/03/2011Updated: 10/17/2026 · 1 min read

FDA Announces Approval of Medical Devices Collection for Third Party Review Program

Summary

The Food and Drug Administration (FDA) has received approval from the Office of Management and Budget (OMB) to collect information on its Medical Devices; Third Party Review Program Under the Food and Drug Administration Modernization Act, as mandated by the Paperwork Reduction Act of 1995.

Original source language: Federal Register — Health and Human ServicesOpen original release →

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