Policies and Guidance

• Is it human research?
  • View decision chart to help determine
• Human research self-certification form
• How do I begin?

Feel free to contact the IRB office for assistance or for “pre-review” of your submission documents.

Policies and procedures

• Unanticipated problems reporting
• Assent policy
• Chart review
• Case report
• Noncompliance
• Policies and procedure manual
• IRB rosters policy
  
  • Click here for PDF
• External IRB review

Guidelines

• Developing a protocol
• Investigator's responsibilities
• Recruitment and retention

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 - PDF

Miscellaneous

• Lay medical terminology
• 10 Things to Speed up IRB Review Time - The IRB has identified the most common omissions and deficiencies in submissions. Attention to these details “up front” should speed the review of your protocols.