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IRB Forms & Templates
Last Updated 1 year 6 months ago
The IRB has implemented the eIRB system. The eIRB Portal which provides access to the system. eIRB has been mandatory since August 2009 for all new submissions and all continuing reviews of approved studies. All active studies are in the eIRB system. The IRB therefore, no longer relies on paper forms. However, the IRB still requires written protocols, consent forms and several other documents
For descriptive, observational studies, registries, treatment INDs & clinical trials.
Consent, signature page, and stand-alone HIPAA authorization templates.
Short Form Consent templates in several languages to use as part of the short form consent process.
This page maintains the few paper forms still required for IRB submissions.