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Journal Abstract Search

178 related items for PubMed ID: 11656894

  • 1. Federal agency proposal will lead to more children serving as research subjects.
    Maloney DM.
    Hum Res Rep; 1997 Oct; 12(10):1-2. PubMed ID: 11656894
    [No Abstract] [Full Text] [Related]

  • 2. Proposal on waiver of informed consent poses major issues for research ethics.
    Maloney DM.
    Hum Res Rep; 1997 Sep; 12(9):1-3. PubMed ID: 11660533
    [No Abstract] [Full Text] [Related]

  • 3. An IRB member's perspective on access to innovative therapy.
    Moore DL.
    Albany Law Rev; 1994 Sep; 57(3):559-81. PubMed ID: 11652854
    [No Abstract] [Full Text] [Related]

  • 4. Informed consent: the FDA's perspective.
    Bagley G.
    Food Drug Law J; 1993 Sep; 48(2):181-6. PubMed ID: 11653141
    [No Abstract] [Full Text] [Related]

  • 5. IRB review of adverse events in investigational drug studies.
    Prentice ED, Gordon B.
    IRB; 1997 Sep; 19(6):1-4. PubMed ID: 11656910
    [No Abstract] [Full Text] [Related]

  • 6. Regulatory orphans: juvenile prisoners as transvulnerable research subjects.
    Reed JG.
    IRB; 1999 Sep; 21(2):9-14. PubMed ID: 11657875
    [No Abstract] [Full Text] [Related]

  • 7. The IRB's role in assessing the generalizability of non-NIH-funded clinical trials.
    Weijer C.
    IRB; 1998 Sep; 20(2-3):1-5. PubMed ID: 11656912
    [No Abstract] [Full Text] [Related]

  • 8. Regulation of clinical research: who's protecting who from what?
    Petricciani JC.
    Food Drug Cosmet Law J; 1979 Apr; 34(4):205-7. PubMed ID: 11661718
    [No Abstract] [Full Text] [Related]

  • 9. Federal agency's final rule says informed consent forms must be dated.
    Maloney DM.
    Hum Res Rep; 1996 Dec; 11(12):1-2. PubMed ID: 11655034
    [No Abstract] [Full Text] [Related]

  • 10. New policy on research with children is part of trend toward including more research subjects.
    Maloney DM.
    Hum Res Rep; 1998 May; 13(5):1-2. PubMed ID: 11657189
    [No Abstract] [Full Text] [Related]

  • 11. Commission says institutional review boards should change procedures now.
    Maloney DM.
    Hum Res Rep; 1999 Jan; 14(1):1-2. PubMed ID: 11657555
    [No Abstract] [Full Text] [Related]

  • 12. The Food and Drug Administration's role in the protection of human subjects.
    Nightingale SL.
    IRB; 1983 Jan; 5(1):6-9. PubMed ID: 11649511
    [No Abstract] [Full Text] [Related]

  • 13. National commission proposes numerous new regulations of institutional review boards.
    Maloney DM.
    Hum Res Rep; 1998 Oct; 13(10):1-2. PubMed ID: 11657739
    [No Abstract] [Full Text] [Related]

  • 14. FDA revises informed consent regulations for emergency research.
    Menasché A, Levine RJ.
    IRB; 1995 Oct; 17(5-6):19-22. PubMed ID: 11653359
    [No Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. An overview of FDA, IRBs and regulations.
    Petricciani JC.
    IRB; 1981 Dec; 3(10):1-3, 11. PubMed ID: 11649413
    [No Abstract] [Full Text] [Related]

  • 17. Emergency trials 'by popular consent.
    Kiernan V.
    New Sci; 1995 Nov 04; 148(2002):6. PubMed ID: 11656475
    [No Abstract] [Full Text] [Related]

  • 18. Considering experimentation and elusive truth: informed consent made difficult.
    Brodeur D.
    Issues (St Louis Mo); 1992 Nov 04; 7(2):1-8. PubMed ID: 11659444
    [No Abstract] [Full Text] [Related]

  • 19. 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]

  • 20. FDA's new rule on treatment use and sale of investigational new drugs.
    Levine RJ.
    IRB; 1987 Oct 01; 9(4):1-4. PubMed ID: 11649946
    [No Abstract] [Full Text] [Related]

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