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IRB Policies and Procedures
An Institutional Review Board is a committee designated by an institution to review, approve the initiation of, and conduct periodic review of research involving human subjects. Human subjects research also includes research that only involves the analysis of identifiable private information on living individuals. The primary purpose of an IRB review is to help assure the protection of the rights and welfare of human subjects. Investigators also share the responsibility for protecting human subjects. The ethical principals described in the Belmont Report provide the foundation for the Federal regulations. The IRB Policies and Procedures are listed below.
University of Maryland System Policy on Human Subjects of Research
University Responsibility for Research Involving Human Subjects
IRB Meeting Dates for Full Board Review
IRB Application Review Process
Submitting an Addendum (Protocol Modification) Request
IRB Staff Contact Information When is IRB Review Required? IRB Policies and Procedures IRB Meeting Dates IRB Membership Roster IRB Applications, Consent Forms and Addendum Requests Student Research Projects FAQs HIPAA Information NIH Certification IRB Training Federal Wide Assurance Federal Regulations and Codes and Requirements for International Research Information Resources
This page is maintained by the UM Division of Research and Graduate Studies. Questions, comments, and/or suggestions should be directed to IRB@deans.umd.edu Institutional Review Board, 2100 Lee Building, University of Maryland, College Park, MD 20742 USA This page last modified 01 March 2006
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