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Journal Abstract Search
627 related items for PubMed ID: 6643032
1. Federal commissions and local IRBs. Yesley MS. Hastings Cent Rep; 1983 Oct; 13(5):11-2. PubMed ID: 6643032 [Abstract] [Full Text] [Related]
2. Looking back at the President's Commission. Capron AM. Hastings Cent Rep; 1983 Oct; 13(5):7-10. PubMed ID: 6580285 [Abstract] [Full Text] [Related]
3. The President's Commission: do we need a sequel? Bunker JP, Fowles J. Hastings Cent Rep; 1983 Oct; 13(5):10-1. PubMed ID: 6580284 [Abstract] [Full Text] [Related]
4. Protection of human subjects. United States. Code Fed Regul Shipping; 1982 Oct 01; Part 46, Sections 46.101 to 46.306():. PubMed ID: 11660819 [No Abstract] [Full Text] [Related]
5. Protection of human subjects: first biennial report on the adequacy and uniformity of federal rules and policies, and their implementation for the protection of human subjects in biomedical and behavioral research; Report of the President's Commission for the Study of Ethical Problems in Medicine and Biomedical and Behavioral Research. Department of Health and Human Services. Notice of report for public comment. Fed Regist; 1982 Mar 29; 47(60):13272-305. PubMed ID: 10298467 [Abstract] [Full Text] [Related]
6. The institutional review board and beyond: future challenges to the ethics of human experimentation. Edgar H, Rothman DJ. Milbank Q; 1995 Mar 29; 73(4):489-506. PubMed ID: 7491097 [Abstract] [Full Text] [Related]
7. National commission proposes numerous new regulations of institutional review boards. Maloney DM. Hum Res Rep; 1998 Oct 29; 13(10):1-2. PubMed ID: 11657739 [No Abstract] [Full Text] [Related]
8. The National Commission on IRBs: an evolutionary approach. Veatch RM. Hastings Cent Rep; 1979 Feb 29; 9(1):22-8. PubMed ID: 429058 [No Abstract] [Full Text] [Related]
9. Special informed consent requirements are included in protocol review procedures. Maloney DM. Hum Res Rep; 1995 Jul 29; 10(7):1-2. PubMed ID: 11654274 [No Abstract] [Full Text] [Related]
10. Commission says institutional review boards should change procedures now. Maloney DM. Hum Res Rep; 1999 Jan 29; 14(1):1-2. PubMed ID: 11657555 [No Abstract] [Full Text] [Related]
11. American Society of Clinical Oncology policy statement: oversight of clinical research. American Society of Clinical Oncology. J Clin Oncol; 2003 Jun 15; 21(12):2377-86. PubMed ID: 12721281 [Abstract] [Full Text] [Related]
12. IRBs and pharmaceutical company funding of research. Jellinek MS, Levine RJ. IRB; 1982 Oct 15; 4(8):9-10. PubMed ID: 11651693 [No Abstract] [Full Text] [Related]
13. Institutional review boards (IRBs) failed to use steps to protect vulnerable research subjects. Maloney DM. Hum Res Rep; 2003 Jun 15; 18(6):6-7. PubMed ID: 15119342 [No Abstract] [Full Text] [Related]
14. Fetal research: the state of the question. Fletcher JC, Schulman JD. Hastings Cent Rep; 1985 Apr 15; 15(2):6-12. PubMed ID: 4008241 [Abstract] [Full Text] [Related]
15. Additional protections for children involved as subjects in research--Department of Health and Human Services. Final rule. Fed Regist; 1983 Mar 08; 48(46):9814-20. PubMed ID: 10259817 [Abstract] [Full Text] [Related]
16. Multicenter trials and subject eligibility: should local IRBs play a role? Freedman B. IRB; 1994 Mar 08; 16(1-2):1-6. PubMed ID: 11652320 [No Abstract] [Full Text] [Related]
17. The standard of disclosure in human subject experimentation. Morin K. J Leg Med; 1998 Jun 08; 19(2):157-221. PubMed ID: 9658739 [No Abstract] [Full Text] [Related]
18. IRB review of adverse events in investigational drug studies. Prentice ED, Gordon B. IRB; 1997 Jun 08; 19(6):1-4. PubMed ID: 11656910 [No Abstract] [Full Text] [Related]
20. Final regulations amending basic HHS policy for the protection of human research subjects--Department of Health and Human Services. Final rule. Fed Regist; 1981 Jan 26; 46(16 Pt 2):8366-91. PubMed ID: 10249932 [Abstract] [Full Text] [Related] Page: [Next] [New Search]