Institutional Review Board
The Institutional Review Board (IRB) ensures that research involving human subjects is conducted ethically and in
compliance with institutional and regulatory standards. This page provides an overview
of the IRB process and requirements.
Frequently Asked IRB Questions
What is the purpose of the IRB?
The Institutional Review Board (IRB) ensures that all research involving human subjects
is conducted ethically and is in compliance with federal regulations and institutional
policies. Its role is to protect the participants and promote responsible research
projects.
Who needs to submit an IRB Application?
Any faculty, staff or student conducting research that involves human participants
must submit an IRB application before beginning the study. This includes surveys,
interviews, experiments, and observational research.
How long does an IRB review take?
Review times vary depending on the type of complexity of the research. Minimal-risk
studies often receive approval within 2–3 weeks, while a full board review may take
4–6 weeks.
What documents are required for submission?
Typical requirements include a completed IRB application form, research protocol,
consent forms, recruitment materials, and any surveys or interview questions.
Can I make changes to my research after IRB submission?
Minor changes may be submitted as amendments for review. Major changes affecting participant
safety, study design, or consent require a full review and re-approval before implementation.
Do student research projects require faculty supervision for IRB approval?
Yes, all student-led research projects must have a faculty advisor or principal investigator
listed on the application to ensure proper oversight.