Letters1 July 2003The Cost of Institutional Review Board Procedures in Multicenter Observational ResearchKeith Humphreys, PhD, Jodie Trafton, PhD, and Todd H. Wagner, PhDKeith Humphreys, PhDPalo Alto Veterans Affairs Medical Center; Stanford University Medical Center (Humphreys, Trafton, Wagner), Jodie Trafton, PhDPalo Alto Veterans Affairs Medical Center; Stanford University Medical Center (Humphreys, Trafton, Wagner), and Todd H. Wagner, PhDPalo Alto Veterans Affairs Medical Center; Stanford University Medical Center (Humphreys, Trafton, Wagner)Author, Article, and Disclosure Informationhttps://doi.org/10.7326/0003-4819-139-1-200307010-00021 SectionsAboutFull TextPDF ToolsAdd to favoritesDownload CitationsTrack CitationsPermissions ShareFacebookTwitterLinkedInRedditEmail TO THE EDITOR:Background: In recent years, there has been significant controversy over how institutional review board (IRB) procedures are structured, administered, and balanced against other concerns (for example, the feasibility of multicenter research) (1). Formal economic analysis has been largely absent in these debates. With hospitals and research facilities under budgetary pressures, it is essential that cost-effective IRB systems be developed.Objective: To estimate the cost of IRB procedures in an eight-site observational substance abuse treatment study.Methods and Findings: We estimated the cost of each IRB action (initial reviews, continuing reviews, amendments, and adverse event reports) at each ...References1. Burman WJ, Reves RR, Cohn DL, Schooley RT. Breaking the camel's back: multicenter clinical trials and local institutional review boards. Ann Intern Med. 2001;134:152-7. [PMID: 11177319] LinkGoogle Scholar2. Wagner TH, Bhandari A, Chadwick GL, Nelson DK. The cost of operating institutional review boards (IRBs). Acad Med 2003; 178: [In press]. Google Scholar3. Christian MC, Goldberg JL, Killen J, Abrams JS, McCabe MS, Mauer JK, . A central institutional review board for multi-institutional trials. N Engl J Med. 2002;346:1405-8. [PMID: 11986418] CrossrefMedlineGoogle Scholar4. New beryllium IRB. Department of Energy. Protecting Human Subjects. 2001-02; Winter:1, 6-7. Accessed at www.science.doe.gov/ober/humsubj/winter01.pdf on 13 June 2002. Google Scholar5. Middle C, Johnson A, Petty T, Sims L, Macfarlane A. Ethics approval for a national postal survey: recent experience. BMJ. 1995;311:659-60. [PMID: 7549633] CrossrefMedlineGoogle Scholar Author, Article, and Disclosure InformationAffiliations: Palo Alto Veterans Affairs Medical Center; Stanford University Medical Center (Humphreys, Trafton, Wagner)Grant Support: By the Department of Veterans Affairs Health Services Research and Development Service. PreviousarticleNextarticle Advertisement FiguresReferencesRelatedDetailsSee AlsoBreaking the Camel's Back: Multicenter Clinical Trials and Local Institutional Review Boards William J. Burman , Randall R. Reves , David L. Cohn , and Robert T. Schooley The Rise of Litigation in Human Subjects Research Michelle M. Mello , David M. Studdert , and Troyen A. 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