摘要
ENSURING INFORMED CONSENT from patients and experimental subjects is today considered normal clinical practice and an essential part of biomedical research involving human subjects. However, 'informed consent' is a technical term from the spheres of ethics and law as developed against a Western cultural background and, as a concept, is still relatively new to China.
ENSURING INFORMED CONSENT from patients and experimental subjects is today considered normal clinical practice and an essential part of biomedical research involving human subjects. However, “informed consent” is a technical term from the spheres of ethics and law as developed against a Western cultural background and, as a concept, is still relatively new to China.Informed consent includes researchers, clinical doctors,
