Informed consent.
Prior to participating in a clinical trial, you have the right to know and understand what will happen from start to finish during the clinical trial process. This is called informed consent and will help you decide whether or not to participate in the study.
A WVU CPRC staff member will explain in detail the informed consent form for each process prior to participant signature acceptance. Prior to signing the consent form you will also be given the opportunity to ask any questions. Our qualified staff members and physician are prepared to answer all questions from potential participants. The Western Institutional Review Board (WIRB), a group of people to independently review research, is available to answer any additional concerns or questions you may have.
It is your right and responsibility to learn as much as possible about any research study you might want to participate in. This information will help you to make an informed decision. It is also your right to withdraw participation/consent at any time, before or after the study has started.