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Journal Abstract Search

409 related items for PubMed ID: 11654269

  • 1. The case of two devices: disclosure to subjects following Phase IV ("post-marketing") research.
    Anderson JR, Jameton A, Reitemeier PJ, Prentice E.
    IRB; 1995; 17(3):6-9. PubMed ID: 11654269
    [No Abstract] [Full Text] [Related]

  • 2. Informed consent in the clinical research setting: experimentation on human subjects.
    Owens JF.
    Med Trial Tech Q; 1987; 33(3):335-50. PubMed ID: 11653829
    [No Abstract] [Full Text] [Related]

  • 3. Informed consent in human experimentation: bridging the gap between ethical thought and current practice.
    Delgado R, Leskovac H.
    UCLA Law Rev; 1986 Oct; 34(1):67-130. PubMed ID: 11659049
    [No Abstract] [Full Text] [Related]

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

  • 5. All is not well in research on human subjects.
    Goldman J.
    N Y Times Web; 1986 Mar 06; ():A26. PubMed ID: 11647822
    [No Abstract] [Full Text] [Related]

  • 6. Balancing moral principles in federal regulations on human research.
    Ackerman TF.
    IRB; 1992 Mar 06; 14(1):1-6. PubMed ID: 11652041
    [No Abstract] [Full Text] [Related]

  • 7. Annual review: observed deficiencies and suggested corrections.
    Adams MS, Conrad DA.
    IRB; 1996 Mar 06; 18(6):1-4. PubMed ID: 11654743
    [No Abstract] [Full Text] [Related]

  • 8. IRBs and pharmaceutical company funding of research.
    Jellinek MS, Levine RJ.
    IRB; 1982 Oct 06; 4(8):9-10. PubMed ID: 11651693
    [No Abstract] [Full Text] [Related]

  • 9. The concept of the IRB and bureaucratic reality: an exchange of letters.
    van Eys J, Levine RJ.
    IRB; 1984 Oct 06; 6(4):8-10. PubMed ID: 11649563
    [No Abstract] [Full Text] [Related]

  • 10. Institutional review boards in the university setting: review of pharmaceutical testing protocols, informed consent and ethical concerns.
    Kobasic DM.
    J Coll Univ Law; 1988 Oct 06; 15(2):185-216. PubMed ID: 11659168
    [No Abstract] [Full Text] [Related]

  • 11. Faith (healing), hope and charity at the FDA: the politics of AIDS drug trials.
    Annas GJ.
    Villanova Law Rev; 1989 Sep 06; 34(5):771-97. PubMed ID: 11651162
    [No Abstract] [Full Text] [Related]

  • 12. The changing clinical trials scene: the role of the IRB.
    Mitchell SC, Steingrub J.
    IRB; 1988 Sep 06; 10(4):1-5. PubMed ID: 11650078
    [No Abstract] [Full Text] [Related]

  • 13. Considering experimentation and elusive truth: informed consent made difficult.
    Brodeur D.
    Issues (St Louis Mo); 1992 Sep 06; 7(2):1-8. PubMed ID: 11659444
    [No Abstract] [Full Text] [Related]

  • 14. Informed consent: the FDA's perspective.
    Bagley G.
    Food Drug Law J; 1993 Sep 06; 48(2):181-6. PubMed ID: 11653141
    [No Abstract] [Full Text] [Related]

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  • 16. Protecting research subjects after consent: the case for the "research intermediary.
    Reiser SJ, Knudson P.
    IRB; 1993 Sep 06; 15(2):10-1. PubMed ID: 11651567
    [No Abstract] [Full Text] [Related]

  • 17. Informed consent process is deemed "legally and ethically invalid" by witness.
    Maloney DM.
    Hum Res Rep; 1995 Jan 06; 10(1):4-5. PubMed ID: 11660008
    [No Abstract] [Full Text] [Related]

  • 18. Issues related to the protection of human research participants.
    Harrison L.
    J Neurosurg Nurs; 1993 Jun 06; 25(3):187-93. PubMed ID: 11660053
    [No Abstract] [Full Text] [Related]

  • 19.
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  • 20. Bill of rights for research subjects.
    Prentice ED, Reitemeier PJ, Antonson DL, Kelso TK, Jameton A.
    IRB; 1993 Jun 06; 15(2):7-9. PubMed ID: 11651568
    [No Abstract] [Full Text] [Related]

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