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62. The politics of informed consent. Weston HB. Natl Forum; 1978; 58(4):23-6. PubMed ID: 11661867 [No Abstract] [Full Text] [Related]
63. FDA seeks public comment on informed consent rules in combat situations. Hastings Cent Rep; 1997; 27(5):43. PubMed ID: 11645003 [No Abstract] [Full Text] [Related]
64. Constraints on experimentation: protecting children to death. Holder AR. Yale Law Policy Rev; 1988; 6(1):137-56. PubMed ID: 11650241 [No Abstract] [Full Text] [Related]
65. IRBs and research with human biological materials. Maloney DM. Hum Res Rep; 1999 Jan; 14(1):2. PubMed ID: 11657556 [No Abstract] [Full Text] [Related]
66. Informed consent to participate in research: Part II. Levine RJ. Bioethics Dig; 1977 Apr; 1(12):1-16. PubMed ID: 11664810 [No Abstract] [Full Text] [Related]
67. Non-therapeutic medical research involving human subjects. Bloom MJ. Syracuse Law Rev; 1973 Apr; 24():1067-1099. PubMed ID: 11664224 [No Abstract] [Full Text] [Related]
68. Institutional review boards and public health research: an analysis. Hogue LL. Univ Ark Little Rock Law J; 1978 Apr; 1(2):428-54. PubMed ID: 11661619 [No Abstract] [Full Text] [Related]
69. A look at the bioresearch monitoring program: the agency perspective. Brisson EL. Food Drug Cosmet Law J; 1983 Apr; 38(2):184-9. PubMed ID: 11649578 [No Abstract] [Full Text] [Related]
70. Multicenter trials and subject eligibility: should local IRBs play a role? Freedman B. IRB; 1994 Apr; 16(1-2):1-6. PubMed ID: 11652320 [No Abstract] [Full Text] [Related]
71. Are clinical trials of cell transplantation for Duchenne muscular dystrophy ethical? Cho MK. IRB; 1994 Apr; 16(1-2):12-5. PubMed ID: 11652321 [No Abstract] [Full Text] [Related]
72. Using the brain dead for medical research. Martyn SR. Utah Law Rev; 1986 Apr; 1986(1):1-28. PubMed ID: 11651917 [No Abstract] [Full Text] [Related]
73. Research involving children: an interpretation of the new regulations. Levine RJ. IRB; 1983 Apr; 5(4):1-5. PubMed ID: 11649521 [No Abstract] [Full Text] [Related]
74. If a subject incurs obligations and carries them out, then consent is a contract: Dahl v. HEM Pharmaceuticals (Part II). Maloney DM. Hum Res Rep; 1996 Jan; 11(1):4-5. PubMed ID: 11653221 [No Abstract] [Full Text] [Related]
75. IRB review of a Phase II randomized clinical trial involving incompetent patients suffering from severe closed head injury. Prentice ED, Antonson DL, Leibrock LG, Kelso TK, Sears TD. IRB; 1993 Jan; 15(5):1-7. PubMed ID: 11659703 [No Abstract] [Full Text] [Related]
76. Human experimentation: the review process in practice. Cowan DH. Case West Reserve Law Rev; 1975 Jan; 25(3):533-64. PubMed ID: 11661165 [No Abstract] [Full Text] [Related]
77. Power, advocacy, and informed consent forms. Smith ML. J Calif Alliance Ment Ill; 1994 Jan; 5(1):25-7. PubMed ID: 11653311 [No Abstract] [Full Text] [Related]