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
ciscrp_officialPartner
Written by
ciscrp_official
Partner
To view profiles and participate in discussions please or .
Read more about...
Not what you're looking for?
You may also like...
Reservations about participating in Clinical Trials...
After reading the book "Bad Pharma" I developed some concerns about participating in Clinical...
Who pays for bad outcomes with Clinical Trials?
Most people who participate in clinical trials do so for either of the following reasons (or some...
Interested in Trials
I'm very interested in trials, but I honestly never hear back from anyone. What is the best way to...
Education Before Participation: What are the different types of clinical trials?
Treatment trials - test new treatments, new combinations of drugs, or new approaches to surgery or...
Why Do People Decide To Participate In Clinical Trials and Why Do People Decide To Continue In A Trial?
I would like to know why people decide to participate in a trial, especially when there are still...
stem cell
Cabozantinib Clinical Trial
