Streamline operations & ensure compliance
If you represent a large research organization such as an academic medical center, cancer center or health system, it can be challenging to maintain compliance and quality assurance across your organization.
Complion ensures that everyone in the organization follows standard processes and procedures, and allows administrators to have visibility into compliance. The platform is configurable to your specifications and robust enough to manage the documentation for hundreds of trials across multiple locations — from any device.
Truly reduce redundancy
The Complion platform allows you to save files once and access them from all of the right places, including through integrations across your other systems.
Investigator-initiated and sponsored trials across multiple internal and external sites? No problem. Advanced IND/IDE and multi-center functionality are included and use the same familiar interface.
Reduce costs, increase reimbursement
Complion allows you to streamline operations and cut costs associated with creating and storing paper binders. Also, fees are reimbursable by your sponsors.
“The ability to document all of the safety-related communications is one of the most important aspects of overseeing the well-being of participants in our research studies. Complion makes it very straightforward to ensure that the right people receive and document that they have read the safety information updates throughout the study. It simplifies the entire process and makes all of our information accessible and organized.”Christy Gilchrist, PhD, CRA, HSHS St. Vincent Hospital