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PUBMED FOR HANDHELDS

Journal Abstract Search

399 related items for PubMed ID: 11657776

  • 1. 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]

  • 2. 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
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  • 4. The concept of the IRB and bureaucratic reality: an exchange of letters.
    van Eys J, Levine RJ.
    IRB; 1984 May; 6(4):8-10. PubMed ID: 11649563
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  • 8. Ethical issues in clinical neurological research.
    Shore D, Berg K, Mullican C.
    J Calif Alliance Ment Ill; 1994 May; 5(1):61-2. PubMed ID: 11653329
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  • 11. Special informed consent requirements are included in protocol review procedures.
    Maloney DM.
    Hum Res Rep; 1995 Jul; 10(7):1-2. PubMed ID: 11654274
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  • 12. Federal investigation concludes that institutional review boards are in trouble.
    Maloney DM.
    Hum Res Rep; 1998 Aug; 13(8):1-2. PubMed ID: 11657190
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  • 18. Federal agency keeps review committee after public comments support continuation.
    Maloney DM.
    Hum Res Rep; 1997 Jan; 12(1):1-2. PubMed ID: 11654603
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  • 20. 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 Jan; 20(1):1-5. PubMed ID: 11655324
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