Is it Human Research? view decision chart to help determine
How to BEGIN?

Adverse Events Reporting Policy
Assent Policy
Guide to Developing a Protocol
Chart Reviews
Guidelines for Recruitment Materials
Investigator Responsibilites
Lay Terminology
Who may give permission for another?
Who may approach patients to seek their participation?
Policies & Procedure Manual
Policy on IRB Rosters
Registering a Clinical Study in a Public Registry
Tracking Changes in a Word document
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. Please feel free to contact the IRB office for assistance or for “pre-review” of your submission documents.