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Business · 27/12/2011Updated: 10/17/2026 · 1 min read

FDA Extends Comment Period for Draft Guidance on Medical Device Clinical Studies

Summary

The Food and Drug Administration (FDA) is extending the comment period for a draft guidance on early feasibility medical device clinical studies, including certain first-in-human studies, to allow more time for public input.

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

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