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Selection of Subjects
Informed Consent T5
Compensation for ResearchInduced Injury
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addition adequate application appropriate approval authority behavior benefits biomedical Chapter Clinical Research clinical trial Commission Commission's committee conducted confidentiality consent form considered deception Declaration of Helsinki determine develop DHEW DHHS diagnostic discussed disease documentation elements of informed ethical example experimental Federal Federal Register fetus harm Hawthorne effect Human Subjects Research identified individual informed consent injury Institutional Review Board institutionalized as mentally investigator involving human subjects IRB members IRB review IRB's justify Lebacqz Levine Medicine mentally infirm minimal risk negotiations for informed nonvalidated Nuremberg Code participation in research patient persons physician practice pregnant presented problems procedures prospective subjects protect protocol psychological purposes reasons Recommendation regulations Report requirements research activities research involving human research subjects responsibility Review of Human rights and welfare role sick role social standard study section Subpart therapeutic therapy tion treatment Tuskegee Syphilis Study vitro fertilization vulnerable