涉及人类受试者的研究

Science (New York, N.Y.)
|September 22, 1978
PubMed
概括

机构审查委员会 (IRB) 通常支持人类受试者保护,但在有效性方面面临批评,特别是在知情同意方面. 他们的行动影响研究建议,但数据表明保护参与者的结果各不相同.

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