The Leading eRegulatory Solution for High-Performing Clinical Research Sites, Sponsors, and CROs

Complion’s platform is the accepted standard built specifically for clinical researchers. Our solution ensures the highest level of compliance with the greatest efficiency and the least amount of work. Allowing you to focus on what really matters — advancing and improving patient outcomes. Whether you are a Research Site, Sponsor or CRO, our eReg solution can help you address any type of clinical trial challenge — now and in the future.


No more paper binders

Reduce costs, avoid redundancy, and increase staff productivity.


Improve efficiency

Easily archive, get eSignatures, and view files from anywhere or from any device.


Audit ready

A built-in audit trail ensures accuracy and eliminates study conduct and patient safety risks.

Complions’ eReg/eISF Platform integrates with WCG IRB Connexus. This integration enables WIRB-Copernicus Group Customers to securely submit and track the management of IRB documentation throughout the entire clinical trial process.

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"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.

What Customers Say

 
HIPAA Compliance
GCP Compliance
FDA Compliance
 

Want to learn more about Complion and our services? Let's talk.