Investigators and study personnel should be familiar with the following policies that relate to human subject protection. Ohio State username (lastname.#) login is required to view or download policies.
Human Research Protections at Ohio State
IRB Submission and Review of 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
- Data and Safety Monitoring
- Event Reporting – Unanticipated Problems Involving Risks to Subjects or Others, Adverse Events, and Other Problems
Special Types of Research
- Research Involving Investigational Drugs
- Research Involving Medical Devices
- Research Involving Data and/or Biospecimens
- Planned Emergency Research
- Emergency Use of Investigational Drugs, Biologics, or Devices
- Collaborative and Multi-site Research
- Research Involving Radiation
- Additional Requirements for Clinical Research: ICH-GCP
- Additional Requirements for Research Sponsored by the Department of Defense (DoD)
- Additional Human Subjects Protection Requirements Based on Federal Agency Funding