Clinical Trail and Human Subject Protection
Developed medicine has a great contribution to the survival of human life and physical and mental health maintenance. The progress of medicine depends on the unremitting study, however, the study of the clinical trials often need to let the physical and mental health and even life of subjects suffered a high degree of risk. Thus, medicine aimed at promoting human well-being could be said to be a nutrient from individual’s sacrifice. In order to ensure the autonomy and safety of subjects in clinical trials, and to strictly obey the principle of informed consent, the trial process is particularly necessary to comply with medical due process, so the risk of the subjects would be under reasonable control. Besides, whether the experimental treatment, which is not entirely belong to medical research and disease treatment, is applicable to medical due process of clinical trials, it’s still be a question. To ensure the patient’s rights and interests, only in the case of the last resort and emergency exception, the physicians have freedom to make decisions of applying and free from the clinical trial for the medical due process of the constraints. In other occasions, there are no different from clinical trials and should be limited by medical due process for clinical trials.