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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

264 related items for PubMed ID: 11649413

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  • 3. The concept of the IRB and bureaucratic reality: an exchange of letters.
    van Eys J, Levine RJ.
    IRB; 1984; 6(4):8-10. PubMed ID: 11649563
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  • 6. FDA revises informed consent regulations for emergency research.
    Menasché A, Levine RJ.
    IRB; 1995; 17(5-6):19-22. PubMed ID: 11653359
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  • 10. The regulation of human experimentation in the United States--a personal odyssey.
    Katz J.
    IRB; 1987; 9(1):1-6. PubMed ID: 11649890
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  • 11. Research compliance changes will affect rules on protection of human subjects.
    Maloney DM.
    Hum Res Rep; 1999 May; 14(5):1-2. PubMed ID: 11657776
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  • 12. OPRR and FDA propose revised expedited review categories.
    McGough H.
    IRB; 1998 May; 20(1):9, 11. PubMed ID: 11655326
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  • 14. IRBs and pharmaceutical company funding of research.
    Jellinek MS, Levine RJ.
    IRB; 1982 Oct; 4(8):9-10. PubMed ID: 11651693
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  • 15. Federal report says protection of human subjects is threatened by numerous factors.
    Maloney DM.
    Hum Res Rep; 1996 May; 11(5):1-3. PubMed ID: 11654438
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  • 16. National commission proposes numerous new regulations of institutional review boards.
    Maloney DM.
    Hum Res Rep; 1998 Oct; 13(10):1-2. PubMed ID: 11657739
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  • 17. Safety boards must report their conclusions to IRBs.
    Maloney DM.
    Hum Res Rep; 1999 Oct; 14(10):3. PubMed ID: 11658061
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  • 18. The paradoxical case of payment as benefit to research subjects.
    Macklin R.
    IRB; 1989 Oct; 11(6):1-3. PubMed ID: 11650284
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  • 19. Federal investigation concludes that institutional review boards are in trouble.
    Maloney DM.
    Hum Res Rep; 1998 Aug; 13(8):1-2. PubMed ID: 11657190
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