News

The Sandbox feature of the eResearch Regulatory Management system has been updated in anticipation of upcoming changes to eResearch. The eResearch Sandbox is an environment in which users may explore...

Clinical study staff can now schedule work and meeting space in our new offices on the fifth floor of University South. Click here to schedule. 

As the weather grows colder and the holiday season approaches, the IRBMED Office would like to remind you that IRBMED will close at the end of business on Wednesday, November 22, and will reopen at...

Major changes to the Common Rule (45 CFR 46 subpart A) are expected to become effective January 19, 2018. IRBMED will approve Amendments and Continuing Review submissions according to 2018 Common...

This comprehensive manual represents the consolidation of the Medical School post-award procedures and best practices.  It is designed to serve the sponsored project post-award community, is based on...

In most instances, federal regulations require that researchers also obtain the permission of each minor subject’s parents or legal guardian. The newest U-MIC presentation summarizes federal and...

IRBMED has updated its guidance on International Council for Harmonisation Good Clinical Practice (ICH-GCP) guidelines. Updates include a revised ICH-GCP checklist. Although researchers are...

All trials that have a billing calendar and/or meet the definition of a UM Clinical Trial are required to enroll in MBECT, Including Clinical trials exempt from completing a billing calendar. ...