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6. The regulation of human experimentation in the United States--a personal odyssey. Katz J IRB; 1987; 9(1):1-6. PubMed ID: 11649890 [No Abstract] [Full Text] [Related]
7. The IRB's role in assessing the generalizability of non-NIH-funded clinical trials. Weijer C IRB; 1998; 20(2-3):1-5. PubMed ID: 11656912 [No Abstract] [Full Text] [Related]
8. Ethical issues in clinical neurological research. Shore D; Berg K; Mullican C J Calif Alliance Ment Ill; 1994; 5(1):61-2. PubMed ID: 11653329 [No Abstract] [Full Text] [Related]
9. Government guinea pigs. Rothman DJ N Y Times Web; 1994 Jan; ():E21. PubMed ID: 11646304 [No Abstract] [Full Text] [Related]
10. The changing clinical trials scene: the role of the IRB. Mitchell SC; Steingrub J IRB; 1988; 10(4):1-5. PubMed ID: 11650078 [No Abstract] [Full Text] [Related]
11. Research compliance changes will affect rules on protection of human subjects. Maloney DM Hum Res Rep; 1999 May; 14(5):1-2. PubMed ID: 11657776 [No Abstract] [Full Text] [Related]
12. Exempt research: procedures in the intramural research program of the National Institutes of Health. Wichman A; Mills D; Sandler AL IRB; 1996; 18(2):3-5. PubMed ID: 11654755 [No Abstract] [Full Text] [Related]
13. The concept of the IRB and bureaucratic reality: an exchange of letters. van Eys J; Levine RJ IRB; 1984; 6(4):8-10. PubMed ID: 11649563 [No Abstract] [Full Text] [Related]
14. Federal report says protection of human subjects is threatened by numerous factors. Maloney DM Hum Res Rep; 1996 May; 11(5):1-3. PubMed ID: 11654438 [No Abstract] [Full Text] [Related]
15. Special informed consent requirements are included in protocol review procedures. Maloney DM Hum Res Rep; 1995 Jul; 10(7):1-2. PubMed ID: 11654274 [No Abstract] [Full Text] [Related]
16. All is not well in research on human subjects. Goldman J N Y Times Web; 1986 Mar; ():A26. PubMed ID: 11647822 [No Abstract] [Full Text] [Related]
17. The quality of mercy. Crigger BJ Hastings Cent Rep; 1993; 23(3):3. PubMed ID: 11643129 [No Abstract] [Full Text] [Related]
18. Toward a more comprehensive approach to protecting human subjects: the interface of data safety monitoring boards and institutional review boards in randomized clinical trials. Gordon VM; Sugarman J; Kass N IRB; 1998; 20(1):1-5. PubMed ID: 11655324 [No Abstract] [Full Text] [Related]
19. NIH guidelines for research involving recombinant DNA molecules. Wilson DJ Account Res; 1993; 3(2-3):177-85. PubMed ID: 11652293 [No Abstract] [Full Text] [Related]
20. American guidance for institutional review boards. Bull Med Ethics; 1998 Nov; No. 143():20-4. PubMed ID: 11657619 [No Abstract] [Full Text] [Related] [Next] [New Search]