Tools and Guides
Researcher Tools
Research/Project Checklists
- Consent/Assent Checklist
- Things to Remember When Conducting Human Subjects Research
- Exempt Project Checklist
- Expedited and Full Board Project Checklist
- Requesting Single Patient Expanded Access
Research Record Templates
- Adverse Event Tracking
- Research Protocol Template
- Consent Discussion Documentation
- Delegation of Responsibilities
- Eligibility Checklist
- Screening/Enrollment Log
- Master Subject List (no consent)
- Visit Checklist
- Pay Documentation Template
- Note-to-File
iMedRIS Guides
(UT NetID and password required)
- Downtime
- Investigator/Coordinator Getting Started Guide
- Routing, Workflow Tracking, and Signoff
- Guide to PI Response Form
- How to Submit a Form 2 - Change Request and Amendments
- How to Submit a Form 3 - Review Continuing Review (Renewal)
- iMedRIS Correspondence
iMedRIS Video Guides
(UT NetID and password required)
- Video Guide - General (Beginner) IRB Training
- Video Guide - Advanced iMedRIS Training
- Video Guide - PI Response Form Submission
- Video Guide - Form 2 Change Request and Amendments
- CTSI: UTHSC Collection of First Informed Consent Date Video
- Watch short videos of iMedRIS version 11.02 revisions/additions (no sound)
Other Tips
Agreements for Collaborations
Consult the IRB Reliance Agreements webpage to download forms and corresponding instructions.