Table of Contents

• IRB Review – What is human subjects research.
• Research Categories
  • Expeditable Research
  • Research Exempt from Full Review
  • Criteria for CUHSR approval of research
  • Not Human Subjects research and Quality Assurance Projects
• Informed Consent
  • General Requirements of Informed Consent
  • Documentation of Consent
  • CUHSR Consent Template for Full and Expedited Studies
  • CUHSR Consent Template for Exempt Studies with Minimal Risk
• Application and Submission Instructions
  • The first page of the application will provide the submission procedure. Imbedded within the application are specific instructions for each section of the application.
• QI/QA CUHSR application form
• Specific Guidelines and Procedures
  • Procedure for Committee Review and Protocol Closure
    • CUHSR Final Status Report and Protocol Closure Form
  • SOTL Research and Human Subjects Protection
  • Guideline for Compensation to Human Research Participants
  • Guideline on Inclusive Language for Researchers Engaging Human Subjects
  • Request for minor modification to a current protocol
  • CUHSR Continuing Review form
• Forms
• Committee Members