On the nature and the Elements of being Informed Consent
Wang Deyan Second Military Medical University,Department of Humanistic and social science,Shanghai,200433,China
Informed consent involves two essential parts:a document and a process.The informed consent document provides a summary of clinical trial(including its purpose,the treatment procedures and schedule,potential risks and benefits,alternative to participation etc.)and explains subject's rights as a participant.The informed consent process provides subjects with ongoing explanations that will help you to make the educated decisions about whether to begin or continue participating in a trial.The article also deals fully with the elements that are explained to subjects.
【CateGory Index】： R-052