The Office of Research Compliance ensures IU conducts its educational, research, and clinical activities in a manner that is consistent with regulatory, statutory, and organizational requirements. This collaborative effort throughout the entire IU community is designed not only to achieve compliance, but also to establish the highest ethical standards governing pre-clinical, clinical, and research activities.
The mission of the Office of Research Compliance is to provide exceptional support for IU's research community in order to catalyze research productivity and protect the institution and its research community from risk.
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Research Integrity Officer
(New CITI Users)
QIO now provides a variety of downloadable templates to assist with both form development and self-auditing, such as: Example Table of Contents for your Regulatory Binder; Informed consent/assent process documentation notes specific to initial consent, reconsent, and for situations requiring use of guardian or LAR in the consent process; Adverse event and protocol deviation tracking - as well as self-audit worksheets for your regulatory binder, drug or device accountability, and subject charts.