Human Subjects Protection Program Policies and Procedures

Table of Contents
Section I: IRB Authority and Institutional Comment
Section II: IRB Compliance Activities
Section III: IRB Review Procedures
Section IV: IRB Informed Consent Process
Section V: Records, Documentation and Fees
Section VI: Investigator Responsibilities
Section VII: IRB Membership
Section VIII: IRB Education and Training
Section IX: Vulnerable Populations
Section X: Conduct of Research
Section XI: Investigational Drugs, Biologics and Devices