Chattanooga IRB Guidance Documents and Policies
IRB Net Instructions
- New User Training Energizer
- Notes for Researchers and Study Coordinators: Submitting a Revised Project Package
- Researcher 1 – New Project Submission
- Researcher 2 – Post Submission Advanced Topics
Policies
- Additional Protections for Children
- Additional Protections for Pregnant Women/Fetuses
- Additional Protections for Prisoners
- Adverse Event Reporting
- Advertisements Policy
- Appeal of IRB Decision
- Auditing Research Studies
- Case Study Reports Policy
- Compassionate Treatment Use
- Conflict of Interests
- Continuing Review
- Criteria for IRB Approval
- Determination Regarding Not Human Subjects Research (NHSR)
- Emergency Use Policy
- Exempt and Expedited Regulations (IRB)
- Expedited Review
- Full Board Review Policy
- Humanitarian Use Devices
- Informed Consent Policy
- Investigator Non-Compliance
- Investigator Responsibilities
- IRB Authority and Membership Policy
- IRB Guidance on Use of PHI Without Subject Authorization
- NHSR Determination Policy
- Non English Speaking Consent Policy
- Privacy and Confidentiality
- Procedures for Full Board Review
- Protocol Waivers Deviations
- Reliance Agreements
- Review of Progress Safety Reports
- Revisions to Studies
- Significant/Nonsignificant Risk Determinations
- Study Closure and Record Retention
- Use of NCI CIRB
- Use of the CIRB