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See why Complion is trusted by hundreds of sites to manage more than 7,000 studies.
Complion streamlines clinical research by enabling sites to manage their regulatory documents in a single platform.
Benefits of Complion:
- No More Binders - Reduce costs and free up office space. Share documents across teams without duplication.
- Improve Efficiency - Easily archive from Outlook, get eSignatures and view files from your phone.
- Audit Ready - Keep everything organized with a built-in audit trail for improved transparency.
- Gain Insight: Easily understand what work has been done and what work still needs to be done.
- Ensure Document Security - Safeguard against deletion, negligence or fraud. Control access and edit permissions across documents and trials.
- Support Investigators - Track all submissions, annual reports, safety reports and correspondence. Coordinate multi-center trials and IITs across external sites.
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Who uses Complion to perform better research?
"Our goal was to streamline our processes and standardize all of our regulatory binders to improve staff training and accessibility across locations. Not only does Complion help us achieve that goal, but it’s also very user friendly and intuitive."
Deborah Tunick, Site Manager
Chesapeake Research Group, LLC