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Business · 22/08/2014Updated: 10/17/2026 · 1 min read

FDA Releases Guidance on Evaluating Sex-Specific Data in Medical Device Clinical Studies

Summary

The FDA has published a guidance document outlining its expectations for the enrollment, analysis, and reporting of sex-specific data in medical device clinical studies, aiming to improve data quality and consistency for devices used in both sexes.

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

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