Contents

• Submissions to the IRB
  • Obtaining an iStar Account
  • CITI (Human Subjects Education
  • Submitting a New Full Board or Expedited Application
  • Submitting a Claim of Exemption
  • Submiting an Amendment to a Previously Approved Protocol
  • Submitting a Continuing Review
  • Submitting a Reportable Event to a Previously Approved Protocol
• Forms and Templates
  • Required Forms and Instructions for IRB Applications
  • Forms for studies conducted at LAC+USC Healthcare Network:
  • Informed Consent Templates and Guidance
  • Experimental Subject's Bill of Rights Templates
  • HIPAA Template and Instructions
  • Other Forms
• Guidance for Researchers
  • Investigators/Research Coordinators
  • Special Types of Research
  • Genetic/Stem Cell Research
  • Biomedical/Clinical Research
  • IRB Reviewer Guidelines
• Info for Med Students
  • The ABC’s of the IRB Process for Student/Medical Student Investigators
  • IRB Training Videos
  • IRB Student Mentor
  • Model IRB Applications
  • Human Subjects Research Brochures
  • Responsible Conduct of Research (RCR)
  • Expedited vs Exempt Studies…perspective of an IRB reviewer
  • Trojan Health Volunteers
• Frequently Asked Questions
  • Why do we have to submit Informed Consent revisions with with tracked changes?
  • How do you Track Changes while you edit?
  • Do I always have to submit a "ROC" form with my IRB application?
  • What do I do if the approval of my study lapses?
• Meetings/Deadlines
  • HSIRB 1 Schedule
  • HSIRB 2 Schedule
  • HSIRB 3 Schedule
• Guidance Index
  • A-D (Accreditation -Decision)
  • E-J (Education-IRB Student Mentor)
  • K-L (Key Personnel-Listserv)
  • M-P (Model IRB Application-Privacy)
  • Q-T (Recruitment-Tissue Repository)
  • U-Z (VA-Waiver of Consent)
• Contact Us/About Us
  • About the HSIRB
  • Contact the HSIRB
  • HSIRB Office Hours
  • HSIRB Administration & Staff
  • HSIRB Membership List

Quick Links

• iStar (IRB Application System)
• CITI (Human Subjects Edu.)
• GCP (Good Clinical Practice)
• HIPAA (Privacy Rule)
• HSPP Policies & Procedures
• FDA | OHRP