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Journal Abstract Search

680 related items for PubMed ID: 11655324

  • 1. 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]

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  • 3. 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]

  • 4. 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]

  • 5. IRBs and randomized clinical trials.
    Meinert CL.
    IRB; 1998 Oct; 20(2-3):9-12. PubMed ID: 11656915
    [No Abstract] [Full Text] [Related]

  • 6. Half-full or half-empty? Evaluating IRB performance.
    Mishkin B, Ariand N.
    Prof Ethics Rep; 1998 Oct; 11(3):4-7. PubMed ID: 11657925
    [No Abstract] [Full Text] [Related]

  • 7. Continuing review of research involving human subjects: approach to the problem and remaining areas of concern.
    Gordon B, Prentice E.
    IRB; 1997 Oct; 19(2):8-11. PubMed ID: 11655323
    [No Abstract] [Full Text] [Related]

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  • 10. The concept of the IRB and bureaucratic reality: an exchange of letters.
    van Eys J, Levine RJ.
    IRB; 1984 Oct; 6(4):8-10. PubMed ID: 11649563
    [No Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. Ethical and legal considerations in dental caries research involving human subjects.
    Branson R.
    J Dent Res; 1980 Jul; 59(Special Issue C):1214-364. PubMed ID: 11651755
    [No Abstract] [Full Text] [Related]

  • 13. Multicenter trials and subject eligibility: should local IRBs play a role?
    Freedman B.
    IRB; 1994 Jul; 16(1-2):1-6. PubMed ID: 11652320
    [No Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. An introduction to NBAC's report on research involving persons with mental disorders that may affect decisionmaking capacity.
    Childress JF.
    Account Res; 1999 Jul; 7(2-4):101-15. PubMed ID: 11658169
    [No Abstract] [Full Text] [Related]

  • 16. Federal investigation concludes that institutional review boards are in trouble.
    Maloney DM.
    Hum Res Rep; 1998 Aug; 13(8):1-2. PubMed ID: 11657190
    [No Abstract] [Full Text] [Related]

  • 17. Institutional animal care and use committees.
    Britt DP.
    ATLA Abstr; 1986 Mar; 13(3):236-9. PubMed ID: 11649839
    [No Abstract] [Full Text] [Related]

  • 18. NIH guidelines for research involving recombinant DNA molecules.
    Wilson DJ.
    Account Res; 1993 Mar; 3(2-3):177-85. PubMed ID: 11652293
    [No Abstract] [Full Text] [Related]

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

  • 20. Proposal for a good clinical practice directive.
    European Commission.
    Bull Med Ethics; 1998 Feb; No. 135():6-11. PubMed ID: 11657249
    [No Abstract] [Full Text] [Related]

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