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Informed Consent and Ethical Review in Chinese Human Experimentation: Reflections on the “Golden Rice Event”
Biotechnology Law Report ( IF 0.2 ) Pub Date : 2014-08-01 , DOI: 10.1089/blr.2014.9979
Xiang Yu , Wei Li

Human experimentation (such as in regard to pharmaceutical efficacy, medical equipment, medical technology, and medical methods) aims to promote the continuous development and application of medical technology so as to improve the human condition.1 Human experimentation involves the interplay of rights and obligations among the sponsor, researcher, and research subjects. In this context, the sponsor is the person or organization that initiates, funds, and supervises the human trials, assuming corresponding responsibilities; the researcher is the physician or scientist who conducts the medical tests; and research subjects are the natural persons who participate in the trials.
更新日期:2014-08-01
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