A single platform for managing regulatory & clinical trial documents.

The documentation burden is only growing for clinical research sites that are buried in paper and binders. Why waste your site’s time and resources manually printing, scanning, and routing documents and correspondence?

 
Complion offers a sponsor-approved, turn-key solution for collecting and managing all of your clinical trial documentation.

Access documents from any device

Create your patient binder, central binder and regulatory binders the same way you always do – but without the hassle. Everything is easily accessible from any device in our cloud-hosted solution.

How it Works
21 CFR Part 11 Compliant

Our platform is 100% Part 11 compliant and meets ICH GCP. Unlike a shared drive, CTMS or sponsor portal, it allows you to control and maintain your documentation entirely electronically.

Part 11 Compliance

Save money

Not only will our solution save you time, but it will most likely cost less than the amount you currently spend on materials and archiving. Even better, it is monitor-accepted and reimbursable.

ROI and Reimbursement
Committed to your success

Our software is user-friendly and we provide exceptional support. Our research certified professionals can get you up and running in a matter of weeks, and you will also have access to the combined knowledge of our customer community.

Why Complion
“What you do really, really well is service and support. You are more than willing to help and provide guidance whenever we need it. Complion is the only vendor we work with that is truly site focused and site driven. We always feel like a priority.”Dustin Caldwell, OptiMed Research

What Customers Say

Join other successful research sites that leverage Complion to manage their clinical trial documentation.

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