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PUBMED FOR HANDHELDS

Journal Abstract Search


309 related items for PubMed ID: 12731493

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  • 3. Time for new rules on human subjects research?
    Dresser R.
    Hastings Cent Rep; 1998; 28(6):23-4. PubMed ID: 9868606
    [No Abstract] [Full Text] [Related]

  • 4. Protecting research subjects--what must be done.
    Shalala D.
    N Engl J Med; 2000 Sep 14; 343(11):808-10. PubMed ID: 10984573
    [No Abstract] [Full Text] [Related]

  • 5. Research involving children: regulations, review boards and reform.
    Gandhi R.
    J Health Care Law Policy; 2005 Sep 14; 8(2):264-330. PubMed ID: 16471026
    [No Abstract] [Full Text] [Related]

  • 6. Reporting problems in human research and resultant investigations by IRBs.
    Maloney DM.
    Hum Res Rep; 2002 Aug 14; 17(8):6-7. PubMed ID: 12731495
    [No Abstract] [Full Text] [Related]

  • 7. Improving protection for research subjects.
    Steinbrook R.
    N Engl J Med; 2002 May 02; 346(18):1425-30. PubMed ID: 11986426
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  • 8. New federal guidance adds duties for institutional review boards (IRBs).
    Maloney DM.
    Hum Res Rep; 2005 Nov 02; 20(11):1-2. PubMed ID: 16358479
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  • 9. Clinical trials face heightened scrutiny as science and commerce appear to merge.
    Lorman AJ.
    J Biolaw Bus; 2001 Nov 02; 4(4):23-32. PubMed ID: 12751494
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  • 10. Institutional review boards and the privacy of human research subjects.
    Maloney DM.
    Hum Res Rep; 2002 Aug 02; 17(8):1-2. PubMed ID: 12731492
    [No Abstract] [Full Text] [Related]

  • 11. Biotech and pharma face more costly clinical trials.
    Brower V.
    Nat Biotechnol; 1998 Aug 02; 16(8):714. PubMed ID: 9702762
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  • 12. The impact of escalating regulatory requirements on the conduct of clinical research.
    Gordon BG, Kessinger A, Mann SL, Prentice ED.
    Cytotherapy; 2003 Aug 02; 5(4):309-13. PubMed ID: 12944237
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  • 13. New privacy rule has more tasks for IRBs.
    Maloney DM.
    Hum Res Rep; 2001 Feb 02; 16(2):4. PubMed ID: 12530379
    [No Abstract] [Full Text] [Related]

  • 14. How institutional review boards (IRBs) can handle adverse event reports.
    Maloney DM.
    Hum Res Rep; 2006 Jan 02; 21(1):1-3. PubMed ID: 16789305
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  • 17. IRBs, data sharing, and privacy of human subjects.
    Maloney DM.
    Hum Res Rep; 2002 Apr 02; 17(4):3. PubMed ID: 12374179
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  • 18. Research infrastructure and IRB/FDA requirements.
    Cohen J.
    Med Health R I; 2000 Dec 02; 83(12):382-5. PubMed ID: 11190124
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