Topical Guidance Fact Sheets
Human Subjects Committee (IRB) General Jurisdiction & Oversight
- Jurisdiction of the HSC
- Activities that Require HSC Review
- Determination of Not Human Subjects Research
- Determination of Quality Assurance or Quality Improvement
- Case Reports & HSC Approval
Human Subjects Committee (IRB) Review
- Federal Criteria of Human Subjects Research
- Types of HSC Review - Quick Reference
- Selecting an HSC Application Form
- Exempt Research
- Expedited Research
- Investigator Initiated Clinical Trials
Informed Consent
- Legally Effective Informed Consent
- Informed Consent Checklist
- Phone Consent
- Consent of Non-English Speaking Subjects
> Instructions for Using Short Form Consent Documentation - Consent Without Subject's Signature
- Consent Involving Surrogate Decision Makers
Collaborative Research
- Collaborative Research and IRB Reciprocity
- Special Arrangements for KUMC (KU Med) - KULC (KU Lawrence) Collaboration
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