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Journal Abstract Search

680 related items for PubMed ID: 11655324

  • 1. Toward a more comprehensive approach to protecting human subjects: the interface of data safety monitoring boards and institutional review boards in randomized clinical trials.
    Gordon VM, Sugarman J, Kass N.
    IRB; 1998; 20(1):1-5. PubMed ID: 11655324
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  • 4. 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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  • 5. IRBs and randomized clinical trials.
    Meinert CL.
    IRB; 1998 Oct; 20(2-3):9-12. PubMed ID: 11656915
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  • 8. The IRB's role in assessing the generalizability of non-NIH-funded clinical trials.
    Weijer C.
    IRB; 1998 Oct; 20(2-3):1-5. PubMed ID: 11656912
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  • 13. Multicenter trials and subject eligibility: should local IRBs play a role?
    Freedman B.
    IRB; 1994 Oct; 16(1-2):1-6. PubMed ID: 11652320
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  • 14. Special informed consent requirements are included in protocol review procedures.
    Maloney DM.
    Hum Res Rep; 1995 Jul; 10(7):1-2. PubMed ID: 11654274
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  • 16. 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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  • 20. Proposal for a good clinical practice directive.
    European Commission.
    Bull Med Ethics; 1998 Feb; No. 135():6-11. PubMed ID: 11657249
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