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Research Article

Using Central IRBs for Multicenter Clinical Trials in the United States

  • Kathryn E. Flynn,

    Affiliations: Duke Clinical Research Institute, Duke University School of Medicine, Durham, North Carolina, United States of America, Department of Psychiatry and Behavioral Sciences, Duke University School of Medicine, Durham, North Carolina, United States of America

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  • Cynthia L. Hahn,

    Affiliation: Office of Research Compliance, Feinstein Institute for Medical Research, North Shore-Long Island Health System, Manhasset, New York, United States of America

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  • Judith M. Kramer,

    Affiliations: Duke Clinical Research Institute, Duke University School of Medicine, Durham, North Carolina, United States of America, Department of Medicine, Duke University School of Medicine, Durham, North Carolina, United States of America

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  • Devon K. Check,

    Affiliation: Duke Clinical Research Institute, Duke University School of Medicine, Durham, North Carolina, United States of America

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  • Carrie B. Dombeck,

    Affiliation: Duke Clinical Research Institute, Duke University School of Medicine, Durham, North Carolina, United States of America

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  • Soo Bang,

    Affiliation: Celgene Corporation, Summit, New Jersey, United States of America

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  • Jane Perlmutter,

    Affiliation: Gemini Group, Ann Arbor, Michigan, United States of America

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  • Felix A. Khin-Maung-Gyi,

    Affiliation: Chesapeake IRB, Columbia, Maryland, United States of America

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  • Kevin P. Weinfurt mail

    kevin.weinfurt@duke.edu

    Affiliations: Duke Clinical Research Institute, Duke University School of Medicine, Durham, North Carolina, United States of America, Department of Psychiatry and Behavioral Sciences, Duke University School of Medicine, Durham, North Carolina, United States of America

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  • Published: January 30, 2013
  • DOI: 10.1371/journal.pone.0054999

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