100 - General Administration
200 - IRB Organization
300 - Functions and Operations
400 - IRB Review of Research
500 - Specific IRB Review Considerations & Categories of Research
600 - IRB Communication with PIs and Other Entities
700 - Informed Consent
800 - Responsibilties of Investigators and Sponsors
900 - Evaluations, Audits, and Non-Compliance
1000 - HIPAA in Research, Privacy and Confidentiality
1100 - Oklahoma State Laws