GeneralBeginner
Informed Consent
Definition
The process by which a participant voluntarily agrees to take part in research after being fully informed about the study's purpose, procedures, risks, benefits, and alternatives.
Example
Before enrolling in a clinical trial, each participant signs a consent form detailing potential side effects and their right to withdraw.
بالعربية
موافقة مسبقة
Related Terms
Use this concept in your research
Heliqy offers 22 research tools to help you apply concepts like informed consent in your medical studies.