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Journal Abstract Search

277 related items for PubMed ID: 11660185

  • 1. Ethical aspects of pharmaceutically-based clinical investigation: report on a national workshop.
    Miller J, Kinsella D, Klein A, Rusted I.
    NCBHR Commun; 1990; 1(1):7-10. PubMed ID: 11660185
    [No Abstract] [Full Text] [Related]

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

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

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

  • 5. Ethics of Research Involving Children: Proceedings of a National Workshop.
    National Council on Bioethics in Human Research (Canada).
    NCBHR Commun; 1993; 4(1):12-41. PubMed ID: 11659941
    [No Abstract] [Full Text] [Related]

  • 6. Institutional review boards in the university setting: review of pharmaceutical testing protocols, informed consent and ethical concerns.
    Kobasic DM.
    J Coll Univ Law; 1988; 15(2):185-216. PubMed ID: 11659168
    [No Abstract] [Full Text] [Related]

  • 7. Ethical issues in clinical neurological research.
    Shore D, Berg K, Mullican C.
    J Calif Alliance Ment Ill; 1994; 5(1):61-2. PubMed ID: 11653329
    [No Abstract] [Full Text] [Related]

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

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

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

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  • 15. Questions and answers.
    Goodwin FK.
    J Calif Alliance Ment Ill; 1994; 5(1):45-7. PubMed ID: 11653321
    [No Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. The Ethics of Human Experimentation: Reinventing the Research Ethics Board: Proceedings of a National Workshop held in Ottawa, Ontario, March 5-6, 1995.
    National Council on Bioethics in Human Research (Canada).
    NCBHR Commun; 1996 Feb; 7(1):5-35. PubMed ID: 11654527
    [No Abstract] [Full Text] [Related]

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  • 19. IRB review of a Phase II randomized clinical trial involving incompetent patients suffering from severe closed head injury.
    Prentice ED, Antonson DL, Leibrock LG, Kelso TK, Sears TD.
    IRB; 1993 Feb; 15(5):1-7. PubMed ID: 11659703
    [No Abstract] [Full Text] [Related]

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

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