IRB Administrative Information
- Board Meetings
- Conflict of Interest Procedures for CWRU Compliance
- Ethics Consultations
- Guidance on Multiple Site Research
- HIPAA Research Policy and Privacy Board
- International Research
- Membership
- Monitoring Audits and Quality Assurance
- Non-Compliance Involving Human Subjects Research
- Receiving and Reviewing Subject Complaints, Concerns, and Questions
- Records
- Reporting to Regulatory Agencies, Department Heads, and Institutional Officials
- Sponsored Projects and Administrative Issues
Investigator Actions
- Certification in Human Subject Protections
- Researcher/Investigator Responsibilities
- Certificate of Confidentiality
New Protocols
- CWRU Comprehensive IRB
- Exempt Research
- Revised Common Rule: CWRU Exemption Categories
- Expedited Review
- Initial Protocol Review and Approval
- Investigational Drugs or Biologics Used in Research
- Investigational Devices Used in Research
- Protocol Submission
- Re-consenting Participants
- Recruitment of Subjects
- Remuneration of Subjects
- Research Involving Chart Reviews
Informed Consent
- Assent from Children
- Informed Consent Guidelines
- Comprehension and the Informed Consent Process
- Re-Obtaining Consent of Subjects
Special Populations in Research
- Special Populations: Children in Research
- Special Populations: Community Based Participatory Research
- Special Populations: Decisionally Impaired Persons
- Special Populations: Other Vulnerable Populations
- Special Populations: Pregnant Women and Neonates
- Special Populations: Prisoners as Research Subjects