Imagine all of your clinical trial documents organized in one place, and accessible wherever you are.

 



As regulatory requirements expand and clinical trials grow more complex, it has become increasingly burdensome for research sites to manage documentation. Complion’s document and workflow management platform improves efficiency, compliance and transparency for research sites and sponsors.



Save time and reduce redundancy:

  • Capture documents and correspondence directly from Outlook
  • Drag and drop files from your computer
  • Fill out an eForm instead of printing and scanning
  • Share documents across teams without duplication
  • With out-of-the-box and customizable integration options



Be ready for an audit anytime:

  • Organize your documents in a familiar “binder” interface to easily search for key information
  • Standardize your “binder” template or create folders on the fly
  • Track all documents and user actions in an automatic audit trail
  • Compile documents in one click to a single formatted PDF

See how Complion pays for itself.

Gain real-time insight into compliance operations:

  • View all binders, documents and outstanding tasks in one place from any device
  • Use keyword search to find what you are looking for
  • Generate configurable reports
  • View and retrieve Complion documents from another system and vice versa



Collaborate to get things done:

  • Assign tasks and track to completion
  • Create user friendly “signature pages” and collect compliant eSignatures from any device
  • Control “binder” access based on role, trial and site or department
  • Share secure access with external sites, CROs and sponsors

Ensure the highest level of security:

  • Create safeguards for improper deletion, negligence, fraud or misconduct
  • Access, maintain, draft or working documents with track-changes in word
  • Control actions and access to documents with configurable user permissions
  • Secure documents with long-term digital archiving options


Support investigators:

  • Provide templates and guidance to meet sponsor requirements
  • Compile documents in the necessary FDA eSubmission formats
  • eSubmit directly from Complion to the FDA
  • Track all submissions, annual reports, safety reports and correspondence
  • Coordinate multi-center investigator-initiated trials across many external sites

What Customers Say

“Our goal was to streamline our processes and standardize all of our regulatory binders to improve staff training and accessibility across locations. Not only does Complion help us achieve that goal, but it’s also very user friendly and intuitive.”Deborah Tunick, Chesapeake Research Group, LLC

Let’s jointly explore the opportunities

Schedule an Interactive Tour