IRB
OSU Human Research Protection Program Policies
| HRPP QUICKLINKS |
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Human Research Protections at OSU
- Human Research Protection Program
- Research Involving Human Subjects
- Noncompliance
- HRPP Policies and Procedures
- HRPP Quality Improvement Activities
IRB Submission and Review of Research
- Exempt Research
- IRB Submission and Pre-Review
- Board Assignment and Reviewer Assignment for Convened Review
- Review of Research by the Convened IRB
- IRB Actions and Communications
- Expedited Review Procedures
- Suspension and Termination of IRB-Approved Research
Study Procedures and Ongoing Research Considerations
- Recruiting Methods, Recruitment Materials, and Participant Compensation
- Privacy and Confidentiality
- Informed Consent Process and the Elements of Informed Consent
- Documentation of the Informed Consent Process
- Assent and Parental Permission
- Short Form Informed Consent
- Event Reporting – Unanticipated Problems Involving Risks to Subjects or Others, Adverse Events, and Other Problems
- Data and Safety Monitoring
Research Involving Special Populations
- Research Involving Pregnant Women, Fetuses, or Neonates
- Research Involving Prisoners
- Research Involving Children
- Vulnerable Populations: Students, Employees, and Adults Unable to Provide Consent
Special Types of Research
- Research Involving Investigational Drugs
- Research Involving Medical Devices
- Research Involving Radiation
- Planned Emergency Research
- Emergency Use of Investigational Drugs, Biologics, or Devices
IRB Operations
- IRB Composition and IRB Member Roles and Responsibilities
- IRB Member and Consultant Conflict of Interest
- IRB Reporting – Unanticipated Problems, Noncompliance, Suspensions, and Terminations
- IRB Recordkeeping
