Institutional Review Board (IRB), General Clinical Research Center at the University of Minnesota

All research projects conducted in the GCRC must be review and approved by the Institutional Review Board (IRB) to ensure protection of the rights and welfare of the research subjects. Investigators are responsible to notify the IRB of any new information that is considered to be relevant to the safety of efficacy of a GCRC protocol for which they are responsible. Documentation of IRB approved GCRC protocols is kept in the GCRC.


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Last modified on Tuesday Apr 12, 2005

This page is located at http://www.med.umn.edu//gcrc/about/irb/home.html