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Business · 24/07/2003Updated: 10/17/2026 · 1 min read

FDA Releases Draft Guidance for Pediatric Medical Devices

Summary

The Food and Drug Administration (FDA) has made available a draft guidance document outlining the agency's requirements for the premarket assessment of pediatric medical devices, aiming to protect vulnerable patient populations during clinical trials.

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

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