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Information you need to know about access to iMedRIS, required training, institutional approval, and submitting an electronic application

Helpful guides to navigating iMedRIS, tools for conducting research, and general tips

Required consent form templates that include specific instructions

Learn about IRB policies and procedures

IRB meeting dates, submission deadlines, and review schedule

Learn about IRB and iMedRIS training opportunities and other resources

IRB fee schedule for research supported by pharmaceutical firms or other for-profit entities

Agreements between the UTHSC IRB and other IRBs or outside investigators

Learn about electronic signatures and whose signatures are required for IRB submissions