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Journal Abstract Search

239 related items for PubMed ID: 11657877

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

  • 2. Advice on compensation: one IRB's response to DHEW's 'interim final regulation'.
    Levine RJ.
    IRB; 1979 Mar; 1(1):5. PubMed ID: 11662737
    [No Abstract] [Full Text] [Related]

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

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

  • 6. IRB review of adverse events in investigational drug studies.
    Prentice ED, Gordon B.
    IRB; 1997 Mar; 19(6):1-4. PubMed ID: 11656910
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  • 9. Institutional review boards in the university setting: review of pharmaceutical testing protocols, informed consent and ethical concerns.
    Kobasic DM.
    J Coll Univ Law; 1988 Mar; 15(2):185-216. PubMed ID: 11659168
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  • 11. 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]

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

  • 13. Bill of rights for research subjects.
    Prentice ED, Reitemeier PJ, Antonson DL, Kelso TK, Jameton A.
    IRB; 1993 Nov 06; 15(2):7-9. PubMed ID: 11651568
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  • 15. Human experimentation: the regulation controversy.
    Society; 1975 Nov 06; 13(1):4-12. PubMed ID: 11662982
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