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Journal Abstract Search

681 related items for PubMed ID: 11651567

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

  • 2. Obtaining "informed consent": controversy over radiation tests focuses attention on rules for human subjects.
    Wheeler DL.
    Chron High Educ; 1994 Jan 26; 40():8-9, 16. PubMed ID: 11658067
    [No Abstract] [Full Text] [Related]

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  • 5. Research subject loses case against physician, IRB, and hospital.
    Maloney DM.
    Hum Res Rep; 1995 Feb 26; 10(2):4-5. PubMed ID: 11654160
    [No Abstract] [Full Text] [Related]

  • 6. Annual review: observed deficiencies and suggested corrections.
    Adams MS, Conrad DA.
    IRB; 1996 Feb 26; 18(6):1-4. PubMed ID: 11654743
    [No Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. Special informed consent requirements are included in protocol review procedures.
    Maloney DM.
    Hum Res Rep; 1995 Jul 01; 10(7):1-2. PubMed ID: 11654274
    [No Abstract] [Full Text] [Related]

  • 9. Bill of rights for research subjects.
    Prentice ED, Reitemeier PJ, Antonson DL, Kelso TK, Jameton A.
    IRB; 1993 Jul 01; 15(2):7-9. PubMed ID: 11651568
    [No Abstract] [Full Text] [Related]

  • 10. Informed consent process is deemed "legally and ethically invalid" by witness.
    Maloney DM.
    Hum Res Rep; 1995 Jan 01; 10(1):4-5. PubMed ID: 11660008
    [No Abstract] [Full Text] [Related]

  • 11. Informed consent in psychiatric research.
    Roth LH, Appelbaum PS, Lidz CW, Benson P, Winslade WJ.
    Rutgers Law Rev; 1987 Jan 01; 39(2-3):425-41. PubMed ID: 11659013
    [No Abstract] [Full Text] [Related]

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

  • 13. Neurobiological research involving human subjects: perspectives from the Office for Protection from Research Risks.
    Puglisi JT, Ellis GB.
    Account Res; 1996 Jan 01; 4(3-4):261-5. PubMed ID: 11654521
    [No Abstract] [Full Text] [Related]

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  • 15. Informed consent to participate in research: Part II.
    Levine RJ.
    Bioethics Dig; 1977 Apr 01; 1(12):1-16. PubMed ID: 11664810
    [No Abstract] [Full Text] [Related]

  • 16. Informed consent process and document is criticized in court.
    Maloney DM.
    Hum Res Rep; 1994 Dec 01; 9(12):4-5. PubMed ID: 11654162
    [No Abstract] [Full Text] [Related]

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

  • 18. NZ medicine after Cartwright.
    Gillett G.
    BMJ; 1990 Apr 07; 300(6729):892-4. PubMed ID: 11642768
    [No Abstract] [Full Text] [Related]

  • 19. The regulation of human experimentation in the United States--a personal odyssey.
    Katz J.
    IRB; 1987 Apr 07; 9(1):1-6. PubMed ID: 11649890
    [No Abstract] [Full Text] [Related]

  • 20. Changing federal regulation of IRB's: the Commission's recommendations and the FDA's proposals.
    Levine RJ.
    IRB; 1979 Mar 07; 1(1):1-3+. PubMed ID: 11662736
    [No Abstract] [Full Text] [Related]

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