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.

NEW! Conflict of Interest: Effective January 1, 2013, the IRB must verify each newly-added member of the research team (Investigator OR Research Personnel) has provided a signed Conflict of Interest/Scientific Misconduct form.

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

Number of Copies: The IRB has transitioned to electronic review of full committee submissions and requires the original versions plus only two (2) photocopies.

2013 Submission Deadlines
IRB Fee Schedule 2009 (Effective for studies submitted 01 Apr 2009 - 01 Jul 2012)
IRB Fee Schedule 2012 (Effective for studies submitted after 01 Jul 2012)

Main Submission Pages:

Initial Submissions
Continuing Review
Completion
Amendments

See Also:

Adverse Events
Advertising / Recruitment
Clinical Trials Listing Form
Conflict of Interest / Scientific Misconduct 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