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**IRB has implemented the use of new application forms,
these must be in use no later than August 1, 2007**
Application for Exemption
Application for Expedited or Full Review (Regular IRB Application)
- If you know that your study does not qualify for an exemption, use this application.
- Completed applications should be submitted to the IRB Office. Please allow ample time to review the application, one to two months.
- Incomplete applications will only be on file for two years from the date of submission.
NIH Human Subjects Training- Training is required for all personnel involved.
Continuation Application for Approved Studies
- Continuation Applications should be submitted to the IRB Office no later than two months before the date of expiration.
- Regular Applications (Expedited or Full Review Applications) expire annually.
- Exemption Applications expire three years from the date of approval.
Informed Consent:
Research information:
Information about the Institutional Review Board:
Federal Documents:
DHHS / OPRR docs - Apply to IRB-regulated studies
FDA docs - Apply to studies that use FDA-regulated drugs, devices or clinical studies
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