Policy Topics:

IRB Purpose, Principles and Responsibilities  - Last revised April 2008
[IRB Policy 001]

IRB Jurisdiction and Authority - Last revised April 2008
[IRB Policy 002]

IRB Composition and Roster - June 2008
[IRB Policy 004]

Research Conflicts of Interest - June 2008
[IRB Policy 007]

IRB General Review Procedures - last revised May 2008
[IRB Policy 008]

Suspension or Termination of IRB Approval of Research - February 2009
[IRB Policy 009]

Off-Site and Cooperative Research - March 2009
[IRB Policy 011]

IRB Record Requirements - September 2008
[IRB Policy 014]

Initial Review of Research - June 2008
[IRB Policy 015]

IRB Quality Assurance Program - April 2009
[IRB Policy 017]

Emergency Use of Drugs, Device and Biologics - NEW December 2009
[IRB Policy 019]

Unanticipated Problems and Adverse Event Reporting - last revised December 2007
[IRB Policy 020] 

Human Subjects Protections Training Requirements -  last revised July 2008
[IRB Policy 021] 

Continuing Review of Approved Research -   last revised December 2007
[IRB Policy 022]

Amendments to Approved Research - June 2008
[IRB Policy 024]

Investigations of Non-Compliance - October 2008
[IRB Policy 026]

Human Subjects Research Determination - December 2008
[IRB Policy 027]

Review of Medical Devices - October 2009
[IRB Policy 031]

We welcome your feedback.  If you wish to provide comments or suggestions on any NSMC IRB policy, or if you have any questions, please contact the IRB Administrator.