Integrate Your Clinical Trial Ecosystem

Complion integrates with WCG solutions to automate clinical trial document flow.

Sponsors, CROs, and Sites are often faced with many bottlenecks and challenges during the clinical trial process. From ineffective site monitoring to a lack of visibility and control into sites. Let’s not forget the ever-present risk of delays in study start up and close out.

These bottlenecks can be overcome as long as you have the right tool that allows you to integrate with other solutions within your clinical trial process.

Complion's eReg/eISF Platform now integrates with WCG IRB Connexus. This integration enables WIRB-Copernicus Group Customers to securely submit and track the management of IRB documentation throughout the entire clinical trial process.

  • More effective remote monitoring
  • Reduce the risk of manual errors and oversight
  • Seamlessly manage the flow of documents without manual intervention


eReg/eISF Solutions for Clinical Trials

› No more paper binders

Reduce costs, avoid redundancy, and increase staff productivity.

› Improved efficiency

Easily archive, get eSignatures, and view files from anywhere or from any device.

› Audit ready

A built-in audit trail ensures accuracy and eliminates study conduct and patient safety risks.