Checklists
IRB members and staff use these checklists to consider and document regulatory items and enhance compliance with federal, state and local requirements.
- HRP-401 – CHECKLIST – Pre-Review
- HRP-402 – CHECKLIST – Non-Committee Review
- HRP-410 – CHECKLIST – Waiver or Alteration of Consent Process
- HRP-411 – CHECKLIST – Waiver of Written Documentation of Consent
- HRP-412 – CHECKLIST – Pregnant Women
- HRP-413 – CHECKLIST – Non-Viable Neonates
- HRP-414 – CHECKLIST – Neonates of Uncertain Viability
- HRP-415 – CHECKLIST – Prisoners
- HRP-416 – CHECKLIST – Children
- HRP-417 – CHECKLIST – Cognitively Impaired Adults
- HRP-418 – CHECKLIST – Non-Significant Risk Device
- HRP-419 – CHECKLIST – Waiver of Consent Process for Emergency Research
- HRP-430 – CHECKLIST – Investigator Quality Improvement
- HRP-431 – CHECKLIST – Minutes Quality Improvement
- HRP-441 – CHECKLIST – HIPAA Waiver of Authorization