Clinical Trials Office
Policies & Procedures
The most current Data Safety Monitoring Plan as well as SRC submission documents and information are located on the Office of Research Administration’s “Forms” page. Once there, click “Indianapolis” and scroll down to the SRC Forms section. There you will find a list of required documents, templates and helpful information regarding protocol submission to the Scientific Review Committee. If you are unable to access this site or have questions, please e-mail email@example.com for more information.