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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 Application Process

IRB Meeting Dates for Full Board Review

IRB Member Directory

IRB Liaisons

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 Liaisons

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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