Review Checklists

The IRB uses these checklists and forms to review protocols for compliance with regulations, policies and guidance:

 Protocol Checklists:

• Protocol - Medical
• Protocol - Expedited (initial review)
• Protocol - Chart Review (initial review)
• Protocol - Non-medical
• Protocol - sIRB Checklist
• SCRO Renewal Review Checklist
• Research Involving VA Studies; see Reviewing Veterans Affairs (VA) Research for additional requirements
• Exemption from IRB Review: Emergency Use of a Test Article
• Single Patient IND/IDE

Other Federal Agency Requirements:

• Dept. of Defense (DoD)
• Dept. of Education (ED)
• Dept. of Energy (DOE)
• Dept. of Justice (DOJ)
• Environmental Protection Agency (EPA)

Informed Consent:

• Informed Consent (medical: clinical studies)
• Informed Consent (medical: expedited/minimal risk)
• Informed Consent (nonmedical: surveys, social, behavioral, education research)
• Neonates

Continuing Review:

• Continuing Review - FULL/EXPEDITED

Reviewer Checklists:

• Medical
• Nonmedical