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
  • Submitting an Application for Not Human Subjects Research (NHSR)
  • Submitting an Amendment to a Previously Approved Protocol
  • Submitting a Continuing Review
• Forms and Templates
  • Informed Consent Templates
  • Other IRB Forms and Templates
  • Additional Human Subjects Research Information and Guidelines for UPC
• Guidance for Researchers
  • Investigators
  • Special Types of Research
  • GWAS/Stem Cell Research
  • Biomedical/Clinical Research
  • IRB Reviewer Guidelines
• Info for 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
  • Where is your office located?
  • What are your office hours?
  • When is your next UPIRB Meeting submission deadline?
  • What is the difference between Expedited and Exempt?
  • What is Not Human Subjects Research (NHSR)?
  • What is the typical turn around time?
  • When does my submission need to go to the Full Board?
  • What do I do if my study has expired? Can I continue collecting data?
  • What if I just found out if I am suppose to have IRB approval before starting research and I already started?
• Meetings/Deadlines
  • Fall 2011 Schedule
  • Spring 2012 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 UPIRB
  • Contact the UPIRB
  • UPIRB Office Hours
  • UPIRB Staff
  • IRB Membership List

Quick Links

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