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Getting Started
Information you need to know about access to iMedRIS, required training, institutional approval, and submitting an electronic application
iMedRIS Login
Log into the electronic IRB system to draft and submit an application, track your submission, or download an IRB-approved document
Tools & Guides
Helpful guides to navigating iMedRIS, tools for conducting research, and general tips
Consent Forms
Required consent form templates that include specific instructions
Standard Operating Procedures
Learn about IRB policies and procedures
Meeting Schedule
IRB meeting dates, submission deadlines, and review schedule
Training & Education
Learn about IRB and iMedRIS training opportunities and other resources
IRB Fees
IRB fee schedule for research supported by pharmaceutical firms or other for-profit entities
IRB Reliance Agreements
Agreements between the UTHSC IRB and other IRBs or outside investigators
Electronic Signatures
Learn about electronic signatures and whose signatures are required for IRB submissions
Noncompliance Concerns
Anonymously report any noncompliance or researcher misconduct concerns
We Want Your Feedback
Take a brief survey about your interaction with the IRB and iMedRIS