Solving Patient Matching in Rare Disease Trials
Apr 29, 2026 - 00:33:36
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In this episode of P4A Let's Talk Rare , hosts Georgie and Owen Bryant from Partners For Access are joined by Wes Michael , founder and president of Rare Patient Voice LLC . Wes shares the organization’s journey from its...
Amplifying Patient Voices: Wes Michael on Rare Disease Advocacy is an episode from Rare Disease, Cell & Gene Therapy Monthly RoundUp by Partners4Access. In this episode of P4A Let's Talk Rare , hosts Georgie and Owen Bryant from Partners Fo...
This episode belongs to Rare Disease, Cell & Gene Therapy Monthly RoundUp.
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Published Oct 10, 2024, 00:23:54 long, audio available.
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