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25. Protocol review within the context of a research program. Miller FG; Rosenstein DL IRB; 1998; 20(4):7-10. PubMed ID: 11657088 [No Abstract] [Full Text] [Related]
26. An attempt to shut down discourse about a controversial practice will not benefit patients, human subjects, the bioethics community, or the research community. Tamar-Mattis A Am J Bioeth; 2010 Sep; 10(9):64-6. PubMed ID: 20818568 [No Abstract] [Full Text] [Related]
27. Dilemmas in paying for clinical research: the view from the IRB. Lind SE IRB; 1987; 9(2):1-5. PubMed ID: 11649900 [No Abstract] [Full Text] [Related]
28. From control to cooperation - Plea for a new role of IRBs. Christen M; Brugger P Cortex; 2015 Oct; 71():415-6. PubMed ID: 26084624 [No Abstract] [Full Text] [Related]
29. [Pediatric research is necessary. The children must be guaranteed with a complete protection]. Dahlquist G Lakartidningen; 2004 Jun; 101(26-27):2238-9. PubMed ID: 15281622 [No Abstract] [Full Text] [Related]
30. The ethical approach to randomization in oncology. Arpaillange P; Dion S Drugs Exp Clin Res; 1986; 12(1-2-3):99-103. PubMed ID: 11650154 [No Abstract] [Full Text] [Related]
31. Research involving children--ethical considerations. Blackhall MI Med J Aust; 1980 Jul; 2(1):1-2. PubMed ID: 7432256 [No Abstract] [Full Text] [Related]
32. Is informed consent always necessary for randomized, controlled trials? Truog RD; Robinson W; Randolph A; Morris A N Engl J Med; 1999 Mar; 340(10):804-7. PubMed ID: 10072420 [No Abstract] [Full Text] [Related]
33. Informed consent to clinical trials in cancer. Lancet; 1982 Jul; 2(8292):275-6. PubMed ID: 6124703 [No Abstract] [Full Text] [Related]
34. Radiation risk and ethical consent. Mountford PJ; Nunan TO Nucl Med Commun; 1995 Jan; 16(1):1-3. PubMed ID: 7609928 [No Abstract] [Full Text] [Related]
35. Research ethics committees--the future. Harris J Not Polit; 2002; 18(67):123-38. PubMed ID: 15282930 [No Abstract] [Full Text] [Related]
36. Multicenter trials and subject eligibility: should local IRBs play a role? Freedman B IRB; 1994; 16(1-2):1-6. PubMed ID: 11652320 [No Abstract] [Full Text] [Related]
37. Widespread IRB-related compliance problems at research institution. Maloney DM Hum Res Rep; 2001 Jan; 16(1):6-7. PubMed ID: 11855427 [No Abstract] [Full Text] [Related]
38. When critical illness interferes with informed consent. Young EW Prog Clin Biol Res; 1989; 299():235-9. PubMed ID: 2657792 [No Abstract] [Full Text] [Related]
39. European guidance on medical research. Council of Europe. Committee of Ministers Bull Med Ethics; 1990 Mar; No. 56():8-10. PubMed ID: 11650345 [No Abstract] [Full Text] [Related]
40. Cognitively impaired subjects. American College of Physicians. Ann Intern Med; 1989 Nov; 111(10):843-8. PubMed ID: 2683918 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]