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2. 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]
3. IRBs and pharmaceutical company funding of research. Jellinek MS, Levine RJ. IRB; 1982 Oct; 4(8):9-10. PubMed ID: 11651693 [No Abstract] [Full Text] [Related]
4. Policies and quality assurance in the pharmaceutical industry. Shamoo AE. Account Res; 1991 Oct; 1(4):273-84. PubMed ID: 11651459 [No Abstract] [Full Text] [Related]
6. The role and responsibility of industry in research. Lasagna L. Dolentium Hominum; 1987 Oct; 4(2nd Yr. 1):56-9. PubMed ID: 11653199 [No Abstract] [Full Text] [Related]
8. Institutional review boards in the university setting: review of pharmaceutical testing protocols, informed consent and ethical concerns. Kobasic DM. J Coll Univ Law; 1988 Oct; 15(2):185-216. PubMed ID: 11659168 [No Abstract] [Full Text] [Related]
9. In search of funding: the clinical investigator and the drug company; Commentary: why researchers need not be demoralized. Siris ES, Burrell CD. IRB; 1983 Oct; 5(6):1-5. PubMed ID: 11649526 [No Abstract] [Full Text] [Related]
14. 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 Oct; 20(1):1-5. PubMed ID: 11655324 [No Abstract] [Full Text] [Related]
15. Money is putting people at risk in biomedical research. Andrews LB. Chron High Educ; 2000 Mar 10; 46(27):B1, B4-5. PubMed ID: 11657699 [No Abstract] [Full Text] [Related]
16. In business to treat cancer. Henig RM. N Y Times Mag; 1986 Nov 23; ():68, 70, 78, 80+. PubMed ID: 11647805 [No Abstract] [Full Text] [Related]