Submissions

Important Notes:

Form revision: The IRB must frequently revise submission forms to ensure that forms contain the most current regulatory requirements. Researchers are encouraged 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 published monthly. Click here to read our newsletters.

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

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