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Abstract: A 6 page paper that explores the ethics of biomedical research, focusing on the key element of voluntary informed consent. Discussed are recent adverse events that have occurred in gene therapy research and the amendments and additions to federal regulations resulting from these events. Also included is a brief discussion of the history of the guidelines and regulations that safeguard human subject volunteers in medical and scientific research. Bibliography lists 8 sources.
Catagory:
Subcatagory: Ethics
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