Economies of Scale in Institutional Review Boards
- 1 August 2004
- journal article
- research article
- Published by Wolters Kluwer Health in Medical Care
- Vol. 42 (8) , 817-823
- https://doi.org/10.1097/01.mlr.0000132395.32967.d4
Abstract
Research with human subjects is essential for most clinical and social science research. As such, the ethical treatment of subjects, including the role of Institutional Review Boards (IRBs), is of paramount concern. The prevailing system of IRBs in the United States reflects an integrated approach in which research organizations have their own local IRB. Recent regulatory changes and a few high-profile problems have prompted proposals for greater investments in IRBs. We conducted regression analyses, looking at how IRB size was associated with IRB costs (economies of scale). We studied data from a cross-sectional survey. We studied IRBs at Veterans Affairs (VA) and VA-affiliated medical centers (n = 109); 81 (73%) IRB administrators completed the survey. Fourteen of the administrators had missing data and were excluded from final analysis, leaving a sample of 67. The primary dependent variable was IRB costs in 2001, which we estimated from the survey. Independent variables included IRB size measured as the number of actions (ie, number of initial reviews, amendments, continuing/annual reviews, and harms/adverse event reports) reviewed by the IRB in the last year. The results indicate that very large economies of scale exist, especially for IRBs that handle fewer than 150 actions per year. A discussion of the costs of benefits of having 3000 to 5000 local IRBs in the United States is warranted because other organizational arrangements could be economically and socially advantageous.Keywords
This publication has 16 references indexed in Scilit:
- A National Survey of Provisions in Clinical-Trial Agreements between Medical Schools and Industry SponsorsNew England Journal of Medicine, 2002
- IRB ReformNew England Journal of Medicine, 2002
- In-Hospital End-of-Life ServicesMedical Care, 2002
- Breaking the Camel's Back: Multicenter Clinical Trials and Local Institutional Review BoardsAnnals of Internal Medicine, 2001
- Assessing Faculty Financial Relationships With IndustryJAMA, 2000
- Protecting Research Subjects — What Must Be DoneNew England Journal of Medicine, 2000
- The Role of Institutional Support in Protecting Human Research SubjectsAcademic Medicine, 2000
- Challenges to Human Subject Protections in US Medical ResearchJAMA, 1999
- Improving Informed Consent in Clinical Trials: A Duty to ExperimentControlled Clinical Trials, 1999
- Updating Protections for Human Subjects Involved in ResearchJAMA, 1998