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Journal Abstract Search

349 related items for PubMed ID: 11655034

  • 1. 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]

  • 2. 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]

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

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

  • 5. 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]

  • 6. 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]

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

  • 8. FDA revises informed consent regulations for emergency research.
    Menasché A, Levine RJ.
    IRB; 1995 Jan; 17(5-6):19-22. PubMed ID: 11653359
    [No Abstract] [Full Text] [Related]

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

  • 10. 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]

  • 11. Emergency trials 'by popular consent.
    Kiernan V.
    New Sci; 1995 Nov 04; 148(2002):6. PubMed ID: 11656475
    [No Abstract] [Full Text] [Related]

  • 12. Protecting research subjects after consent: the case for the "research intermediary.
    Reiser SJ, Knudson P.
    IRB; 1993 Nov 04; 15(2):10-1. PubMed ID: 11651567
    [No Abstract] [Full Text] [Related]

  • 13. Changing federal regulation of IRB's: the Commission's recommendations and the FDA's proposals.
    Levine RJ.
    IRB; 1979 Mar 04; 1(1):1-3+. PubMed ID: 11662736
    [No Abstract] [Full Text] [Related]

  • 14. A look at the bioresearch monitoring program: the agency perspective.
    Brisson EL.
    Food Drug Cosmet Law J; 1983 Apr 04; 38(2):184-9. PubMed ID: 11649578
    [No Abstract] [Full Text] [Related]

  • 15. Two rules on expedited IRB reviews are final.
    Maloney DM.
    Hum Res Rep; 1999 Jan 04; 14(1):3. PubMed ID: 11657557
    [No Abstract] [Full Text] [Related]

  • 16. Proposed requirements for informed consent go beyond current federal regulations.
    Hum Res Rep; 1994 Jul 04; 9(7):1-3. PubMed ID: 11659879
    [No Abstract] [Full Text] [Related]

  • 17. Institutional review board approval required by rule.
    Maloney DM.
    Hum Res Rep; 1996 Aug 04; 11(8):3. PubMed ID: 11654440
    [No Abstract] [Full Text] [Related]

  • 18. 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]

  • 19. Power, advocacy, and informed consent forms.
    Smith ML.
    J Calif Alliance Ment Ill; 1994 Oct 01; 5(1):25-7. PubMed ID: 11653311
    [No Abstract] [Full Text] [Related]

  • 20. The paradoxical case of payment as benefit to research subjects.
    Macklin R.
    IRB; 1989 Oct 01; 11(6):1-3. PubMed ID: 11650284
    [No Abstract] [Full Text] [Related]

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