Human Subject Application Kit

Guidelines (read these before submitting)
     IRB Quick Guide   NEW March 2015
Informed Consent Guidelines
     Informed Consent Form Checklist
     Belmont Report  summarizes basic ethical principles and guidelines identified by the National Commission
             for the Protection of Human Subjects of Biomedical and Behavioral Research to assist in developing
             human subjects review application. 

Application Materials

     IRB Application   REVISED January 2015 (Mac users may experience formatting problems)

Informed Consent Form Template 
Informed Consent Form Template for Online Participants
     Approval Letter from External Organization Example
     Approval Letter from External Organization Example

How to Submit
Prior to the review of any IRB application, all applications including instrumentation must be screened for completeness before it can be cleared for review.  Therefore, IRB applications must FIRST be delivered to the attention of:
    Office of Academic Affairs
    Institutional Review Board
    Siena College, Siena Hall 202
    (518) 783-2307
Once expedited or exempt IRB application has been screened for completeness, the IRB application will be sent to the IRB Chair for review and approval.