Problems in Securing Informed Consent of Subjects in Experimental Trials of Unapproved Drugs and Devices
Washington, DC: Superintendent of Documents, United States Government Printing Office [GPO], 1994. 270 p.
Consent; Drugs; Informed Consent; Drugs and Drug Industry; Human Experimentation Policy Guidelines / Institutional Review Boards; Informed Consent or Human Experimentation; Scientific Research Ethics; Research on Special Populations; Research on Newborns and Minors; Research on Mentally Disabled Persons;
United States. Congress. House. Committee on Small Business. Subcommittee on Regulation, Business Opportunities, and Technology
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