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Journal Abstract Search

234 related items for PubMed ID: 11654523

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

  • 2. Informed consent process and document is criticized in court.
    Maloney DM.
    Hum Res Rep; 1994 Dec; 9(12):4-5. PubMed ID: 11654162
    [No Abstract] [Full Text] [Related]

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

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

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

  • 6. Informed consent to participate in research: Part II.
    Levine RJ.
    Bioethics Dig; 1977 Apr; 1(12):1-16. PubMed ID: 11664810
    [No Abstract] [Full Text] [Related]

  • 7. Neurobiological research involving human subjects: perspectives from the Office for Protection from Research Risks.
    Puglisi JT, Ellis GB.
    Account Res; 1996 Apr; 4(3-4):261-5. PubMed ID: 11654521
    [No Abstract] [Full Text] [Related]

  • 8. Proposal on waiver of informed consent poses major issues for research ethics.
    Maloney DM.
    Hum Res Rep; 1997 Sep; 12(9):1-3. PubMed ID: 11660533
    [No Abstract] [Full Text] [Related]

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

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

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

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

  • 13. Federal agency's final rule says informed consent forms must be dated.
    Maloney DM.
    Hum Res Rep; 1996 Dec; 11(12):1-2. PubMed ID: 11655034
    [No Abstract] [Full Text] [Related]

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

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

  • 16. 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]

  • 17. 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]

  • 18. The FDA's final regulations: IRBs and medical devices.
    Holder AR.
    IRB; 1980 Mar 06; 2(6):1-4. PubMed ID: 11661803
    [No Abstract] [Full Text] [Related]

  • 19. Human experimentation: the regulation controversy.
    Society; 1975 Mar 06; 13(1):4-12. PubMed ID: 11662982
    [No Abstract] [Full Text] [Related]

  • 20. Hospital failed on human research policy.
    Science; 1998 Nov 06; 282(5391):1035. PubMed ID: 11645114
    [No Abstract] [Full Text] [Related]

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