Main Content

Guidance

• Is it human research?
  • View decision chart to help determine
• How do I begin?
• Unanticipated problems reporting
• Assent guidance
• Case report
• IRB Roster Disclosure
• 10 Things to Speed up IRB Review Time

FAQs

• Are you planning to conduct a Genome-Wide Association (GWAS) study?
• Who may give permission for another?
• Who may approach patients to seek their participation?
• What is PHI?
• Single IRB FAQs