Paying it forward in #clinicalresearch. Hear the stories of #clinicaltrial participants who are sharing their experiences with others on Wed. Nov. 10th 12PM EST. Britta Dornan of EveryLife Foundation for Rare Disease moderates. Panelists include Ryan Colburn, #pompedisease advocate, Dr. Kim Stephens of Project Alive & Marc Yale of the International Pemphigus & Pemphigoid Foundation. Register for the webinar today: zoom.us/webinar/register/WN...
Sharing Experiences in Rare Disease C... - Understanding Cli...
Sharing Experiences in Rare Disease Clinical Trials
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