IRB Checklists & Guidance
These checklists are to be used by IRB reviewers to review protocols and by Investigators to assist them in preparing protocols for review:
- Advertisements (210i)
- Contingent Approval (210d)
- Continuing Review Checklist for Reviewers
- Exempt Research (210r)
- Expedited Review Determination Checklist
- Guidance on Requirements of the Sponsor and the Investigator as a Sponsor
- ICH Good Clinical Practices (GCP), Applicability to Human Subjects Research
- Initial Protocol Review Checklist
- Modification Review Checklist
- Non-Human Subject Research Letter and Checklist (Doc 211l)
- Lay Summary Guidance