The Leading eRegulatory Solution for High-Performing Clinical Research Sites, Sponsors, and CROs
No more paper binders
Reduce costs, avoid redundancy, and increase staff productivity.
Easily archive, get eSignatures, and view files from anywhere or from any device.
A built-in audit trail ensures accuracy and eliminates study conduct and patient safety risks.
"With almost all of our staff -- and even some investigators -- completely remote during the pandemic, Complion has helped us remain compliant with obtaining signatures on key regulatory documents in real-time for older, paper-based studies. The Complion team was very fast to help us with a solution to utilize the system for these studies."Ashlee Drawz, Director, Research Oversight & Compliance, Robert H. Lurie Comprehensive Cancer Center, Northwestern University
"As a result of the COVID-19 pandemic, we've had to cancel all monitoring visits (at least non-CRAs), which has made the CRAs even more grateful for Complion!"Brooke Barrick, Regulatory Manager, J. Lewis Research, Inc.