Informed Consent-What is it?
This is a discussion of all procedures, benefits, risks and expectations of a clinical trial between the investigator and people who participate in the study. After being informed about the study and having a chance to ask questions, all participants sign an informed consent form before participating in the research.
Related Questions
- Designated Premises Supervisor Q: When an applicant for a premises licence also wishes to be the Designated Premises Supervisor, do they need to complete the form of consent in Schedule 2 of the application?
- If by law a child is able to consent to treatment without parental permission, can they also consent to participate in research related to that treatment?
- What is the consent provision in cases with health care professional?
