1. Guidance on Exemption Categories under the Revised Common Rule
  2. IRB QI/Program Evaluation Self-Certification Tool Guidance
  3. Guidance on Research vs. Quality Improvement and Program Evaluation
  4. Exemption Guidance
  5. Guidance for the Submission of Investigator's Drug Brochures (IDBs) and Package Inserts
  6. Personnel Change Guidance
  7. Expedited Change of Protocol Guidance
  8. How to Remove Study Team Members
  9. Application Type Guidance
  10. Do I need to get consent for my exempt study?
  11. Guidance on Presenting Changes of Protocol to IRB
  12. Continuing Review: UW-Madison Purview Enrollment Guidance
  13. Vulnerable Populations Guidance
  14. Guidance for Completing IRB Applications for Recruitment Registries or Repositories that Store Data and/or Tissue
  15. Protocol Development Activities (PDA) Guidance