What is an Informed Consent?
The Informed Consent Form is designed to give the potential participant, or their legal representative, easy-to-understand information regarding all aspects of a specific clinical trial. It is designed to provide all the information needed to help a person decide it they want to participate in the trial. Adequate time is allowed to ask questions and to make sure the potential participant feels comfortable with and agrees to the terms of the clinical trial. No study related procedures will be performed until the Informed Consent Form is signed by the participant. Each participant is given a copy of the Informed Consent Form.
Tags: clinical research, medical research, research, Treasure Valley research












