Table of Contents
Does my project require IRB review?
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- Adverse Event Reporting
- Clinicaltrials.gov
- Emergency Treatment
- Exempt Studies
- Incidents (Non-compliance/Problems)
- Protocol Deviations
- Submission Process
- HRPP Investigator Guidance Series
- Investigator Resources
- IRB Conference Content
- Mental Health Considerations
- Miscellaneous Resources
- CITI Training
- Community Partners
- Consent Forms
- E-Signature Instructions
- IRB Training Videos
- RSS Training
- Virtual Training/Office Hours
- Existing Paper Protocols
- FWAs - Federal Wide Assurance
- Miscellaneous
- Recruitment templates
- Short Forms
- Subject's Rights & Responsibilities