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PUBMED FOR HANDHELDS

Journal Abstract Search

653 related items for PubMed ID: 11656540

  • 1. Fears mount for gene scrutiny as watchdog faces axe.
    Kiernan V.
    New Sci; 1996 Jun 08; 150(2033):10. PubMed ID: 11656540
    [No Abstract] [Full Text] [Related]

  • 2. Special informed consent requirements are included in protocol review procedures.
    Maloney DM.
    Hum Res Rep; 1995 Jul 08; 10(7):1-2. PubMed ID: 11654274
    [No Abstract] [Full Text] [Related]

  • 3. Proposed requirements for informed consent go beyond current federal regulations.
    Hum Res Rep; 1994 Jul 08; 9(7):1-3. PubMed ID: 11659879
    [No Abstract] [Full Text] [Related]

  • 4. Review panel cancels meeting as gene therapy proposals fall.
    Wadman M.
    Nature; 1996 Feb 22; 379(6567):668. PubMed ID: 11644770
    [No Abstract] [Full Text] [Related]

  • 5. Commission says institutional review boards should change procedures now.
    Maloney DM.
    Hum Res Rep; 1999 Jan 22; 14(1):1-2. PubMed ID: 11657555
    [No Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. IRB review of adverse events in investigational drug studies.
    Prentice ED, Gordon B.
    IRB; 1997 Oct 01; 19(6):1-4. PubMed ID: 11656910
    [No Abstract] [Full Text] [Related]

  • 8. Gene therapy in mental retardation: ethical considerations.
    Fletcher JC.
    Ment Retard Dev Disabil Res Rev; 1995 Oct 01; 1():7-13. PubMed ID: 11660293
    [No Abstract] [Full Text] [Related]

  • 9. National commission proposes numerous new regulations of institutional review boards.
    Maloney DM.
    Hum Res Rep; 1998 Oct 01; 13(10):1-2. PubMed ID: 11657739
    [No Abstract] [Full Text] [Related]

  • 10. The concept of the IRB and bureaucratic reality: an exchange of letters.
    van Eys J, Levine RJ.
    IRB; 1984 Oct 01; 6(4):8-10. PubMed ID: 11649563
    [No Abstract] [Full Text] [Related]

  • 11. Annual review: observed deficiencies and suggested corrections.
    Adams MS, Conrad DA.
    IRB; 1996 Oct 01; 18(6):1-4. PubMed ID: 11654743
    [No Abstract] [Full Text] [Related]

  • 12. OPRR and FDA propose revised expedited review categories.
    McGough H.
    IRB; 1998 Oct 01; 20(1):9, 11. PubMed ID: 11655326
    [No Abstract] [Full Text] [Related]

  • 13. IRBs and pharmaceutical company funding of research.
    Jellinek MS, Levine RJ.
    IRB; 1982 Oct 01; 4(8):9-10. PubMed ID: 11651693
    [No Abstract] [Full Text] [Related]

  • 14. Beyond localism: a proposal for a National Research Review Board.
    Levine C, Caplan AL.
    IRB; 1986 Oct 01; 8(2):7-9. PubMed ID: 11649751
    [No Abstract] [Full Text] [Related]

  • 15. Federal agency keeps review committee after public comments support continuation.
    Maloney DM.
    Hum Res Rep; 1997 Jan 01; 12(1):1-2. PubMed ID: 11654603
    [No Abstract] [Full Text] [Related]

  • 16. Ethical and legal considerations in dental caries research involving human subjects.
    Branson R.
    J Dent Res; 1980 Jul 01; 59(Special Issue C):1214-364. PubMed ID: 11651755
    [No Abstract] [Full Text] [Related]

  • 17. Human experimentation: the review process in practice.
    Cowan DH.
    Case West Reserve Law Rev; 1975 Jul 01; 25(3):533-64. PubMed ID: 11661165
    [No Abstract] [Full Text] [Related]

  • 18. The regulation of human experimentation in the United States--a personal odyssey.
    Katz J.
    IRB; 1987 Jul 01; 9(1):1-6. PubMed ID: 11649890
    [No Abstract] [Full Text] [Related]

  • 19. The paradoxical case of payment as benefit to research subjects.
    Macklin R.
    IRB; 1989 Jul 01; 11(6):1-3. PubMed ID: 11650284
    [No Abstract] [Full Text] [Related]

  • 20. Using the brain dead for medical research.
    Martyn SR.
    Utah Law Rev; 1986 Jul 01; 1986(1):1-28. PubMed ID: 11651917
    [No Abstract] [Full Text] [Related]

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