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. It ensures the highest level of compliance with the least amount of work, so that you can focus on what really matters – your research trials.

During the COVID-19 pandemic, the burden of work has become even heavier and more pressing. Some clinical researchers have had to hold operations, while others are involved in COVID-19 vaccine trials. Many are trying to continue trials that can’t afford to be stopped amid strict practices of distancing and quarantining.

That’s why we’ve made it our goal to do everything we can to make your work not only easier, but possible, during this period of uncertainty. Whether you are a Research Site, Sponsor or CRO, our eReg solution can help you address your clinical trial challenges during COVID-19, and going forward.

No more paper binders

Reduce costs, avoid redundancy and free up office space.

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.

Our clients include leading cancer centers, medical centers, hospitals and health systems, as well as multi-specialty practices and dedicated research sites

Learn more about our solutions for:

“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