The consent form that you receive when you are invited to be a research subject includes some contact information if you have questions or concerns about the study.
For more information concerning research study(s) and research-related risks or injuries, or to give comments, concerns or complaints, you may contact a representative of the Institutional Review Board (IRB) of for information regarding your rights as a participant involved in a research. You may obtain the name and number of this person by calling (864) 455-8997.
A survey about your experience with this informed consent process is also available.
Participation in the survey is completely anonymous and voluntary and will not affect your relationship with your doctor or Greenville Health System. If you would like to have a paper copy of this survey, please tell your study coordinator.