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 during the COVID-19 pandemic and beyond. Learn about how your site can benefit from leveraging our eReg solution.
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.
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.
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.
Committed to your success
Our software is user-friendly and we provide exceptional support. Our experienced team of eRegulatory professionals can get you up and running quickly, and you will also have access to the combined knowledge of our customer community.
“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