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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

625 related items for PubMed ID: 11660533

  • 21. Issues related to the protection of human research participants.
    Harrison L.
    J Neurosurg Nurs; 1993 Jun; 25(3):187-93. PubMed ID: 11660053
    [No Abstract] [Full Text] [Related]

  • 22. The FDA's enforcement of IRBs and patient informed consent.
    Kelsey FO.
    Food Drug Cosmet Law J; 1989 Jan; 44(1):13-20. PubMed ID: 11651627
    [No Abstract] [Full Text] [Related]

  • 23. Walking a thin line: distinguishing between research and medical practice during Operation Desert Storm.
    Schuchardt EJ.
    Columbia J Law Soc Probl; 1992 Jan; 26(1):77-115. PubMed ID: 11651647
    [No Abstract] [Full Text] [Related]

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

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

  • 26. The FDA's final regulations: IRBs and medical devices.
    Holder AR.
    IRB; 1980 Jan; 2(6):1-4. PubMed ID: 11661803
    [No Abstract] [Full Text] [Related]

  • 27. The changing clinical trials scene: the role of the IRB.
    Mitchell SC, Steingrub J.
    IRB; 1988 Jan; 10(4):1-5. PubMed ID: 11650078
    [No Abstract] [Full Text] [Related]

  • 28. In tests on people, who watches the watchers?
    Hilts PJ.
    N Y Times Web; 1999 May 25; ():F1, F4. PubMed ID: 11648129
    [No Abstract] [Full Text] [Related]

  • 29. Ethics in neurobiological research with human subjects -- final reflections.
    Katz J.
    Account Res; 1996 May 25; 4(3-4):277-83. PubMed ID: 11654523
    [No Abstract] [Full Text] [Related]

  • 30. Informed consent in psychiatric research.
    Roth LH, Appelbaum PS, Lidz CW, Benson P, Winslade WJ.
    Rutgers Law Rev; 1987 May 25; 39(2-3):425-41. PubMed ID: 11659013
    [No Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
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  • 32. The IRB's role in assessing the generalizability of non-NIH-funded clinical trials.
    Weijer C.
    IRB; 1998 May 25; 20(2-3):1-5. PubMed ID: 11656912
    [No Abstract] [Full Text] [Related]

  • 33. An update on the PEG-SOD study involving incompetent subjects: FDA permits an exception to informed consent requirements.
    Prentice ED, Antonson DL, Leibrock LG, Prabhu VC, Kelso TK, Sears TD.
    IRB; 1994 May 25; 16(1-2):16-8. PubMed ID: 11652322
    [No Abstract] [Full Text] [Related]

  • 34. "Evaluation of human subject protections in schizophrenia research conducted by the University of ..." (Part III).
    Maloney DM.
    Hum Res Rep; 2000 Jan 25; 15(1):5-6. PubMed ID: 11658036
    [No Abstract] [Full Text] [Related]

  • 35. Court tells jury to ignore human subject protection regulations.
    Maloney DM.
    Hum Res Rep; 1995 Mar 25; 10(3):4-5. PubMed ID: 11654195
    [No Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
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  • 37. 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]

  • 38. Research subject loses case against physician, IRB, and hospital.
    Maloney DM.
    Hum Res Rep; 1995 Feb 08; 10(2):4-5. PubMed ID: 11654160
    [No Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
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  • 40. IRBs and randomized clinical trials.
    Meinert CL.
    IRB; 1998 Feb 08; 20(2-3):9-12. PubMed ID: 11656915
    [No Abstract] [Full Text] [Related]

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