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CDRH Patient Education Program: Patients as Advisors in Medical Device Clinical Studies

U.S. Food and Drug Administration · June 2, 2026

An FDA-produced online training explains the role of patient advisors in medical device clinical studies, outlines stages of device development, and gives first-person examples of how patient input can shape study design, recruitment, analysis and dissemination.

AI-Generated Content: All content on this page was generated by AI to highlight key points from the meeting. For complete details and context, we recommend watching the full video. so we can fix them.