We understand your pain

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

There’s a better way

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

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

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

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

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

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

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