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.
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.
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.