Rights and Responsibilities in Drug Research: An Examination of the Scope of Ethical, Social, and Legal Rights and Responsibilities of Principal Investigators, Sponsors, Institutional Review Committees, and Government Regulatory Agencies And Funding
Curran, William J.
Washington, DC: Medicine in the Public Interest, 1977. 84 p.
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Draft Guidance for Institutional Review Boards, Clinical Investigators, and Sponsors; Exception From Informed Consent Requirements for Emergency Research: Notice Unknown creator (United States. Food and Drug Administration [FDA], 2006-08-29)
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