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Journal Abstract Search

464 related items for PubMed ID: 11662736

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

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

  • 3. 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]

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

  • 5. Changing federal regulation of IRB's, part II: DHEW's and FDA's proposed regulations.
    Levine RJ.
    IRB; 1979 Nov; 1(7):1-5+. PubMed ID: 11661757
    [No Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. 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]

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

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

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

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

  • 12. 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]

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

  • 14. The IRB's role in assessing the generalizability of non-NIH-funded clinical trials.
    Weijer C.
    IRB; 1998 Dec; 20(2-3):1-5. PubMed ID: 11656912
    [No Abstract] [Full Text] [Related]

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

  • 16. Informed consent to participate in research: Part II.
    Levine RJ.
    Bioethics Dig; 1977 Apr 04; 1(12):1-16. PubMed ID: 11664810
    [No Abstract] [Full Text] [Related]

  • 17. Can (or should) the IRB assume the FDA's functions at early stages of the IND process?
    Levine RJ.
    IRB; 1981 Dec 04; 3(10):4-5. PubMed ID: 11649414
    [No Abstract] [Full Text] [Related]

  • 18. Selective review of external adverse events: one IRB's response to the avalanche of IND safety reports.
    Gordon B, Prentice E.
    IRB; 1999 Dec 04; 21(3):10-1. PubMed ID: 11657877
    [No Abstract] [Full Text] [Related]

  • 19. Informed consent process is deemed "legally and ethically invalid" by witness.
    Maloney DM.
    Hum Res Rep; 1995 Jan 04; 10(1):4-5. PubMed ID: 11660008
    [No Abstract] [Full Text] [Related]

  • 20. The impact of institutional review boards on clinical research.
    Levine RJ.
    Perspect Biol Med; 1995 Jan 04; 23(2):. PubMed ID: 11663073
    [No Abstract] [Full Text] [Related]

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