Submissions

Important Notes:

Form revision: All forms were revised August, 2011. Our goal was to provide more guidance to clarify our questions.

If a researcher has already started to fill in an obsolete form, we will accept the old forms for a few weeks. However, we ask researchers to start using the new forms as soon as possible and to make the transition to the new forms by November, 2011 for all submissions.

We also encourage researchers to download forms from the website each time a form is needed to make sure they are using the most current version.

HIPAA Training: Effective July 1, 2010, all investigators and research staff must provide evidence of research-specific HIPAA training for all initial submissions, continuing reviews, and personnel changes. Click here for instructions to access the free online CITI training program.

IRB Newsletter: IRB Newsletters are now published monthly. Click here to read our newsletters.

2011 Submission Deadlines (xls) (pdf)
2012 Submission Deadlines (xls) (pdf)
IRB Fee Schedule (Effective 01 Apr 2009)

Main Submission Pages:

Initial Submissions
Continuing Review
Completion
Amendments

See Also:

Adverse Events
Advertising / Recruitment
Clinical Trials Listing Form
Exempt Review
Expedited Review
HIPAA Training Certification
Human Subjects Protection Certification
Informed Consent
Personnel Changes
Protocol Amendments
Protocol Deviations
Review Process
Unanticipated Problems
Waivers of Informed Consent and HIPAA Authorization