Complion’s industry-leading eRegulatory document and workflow management platform improves efficiency, compliance and transparency for research sites and sponsors. The sponsor-approved, turn-key platform stores, organizes and routes all of the regulatory documentation involved in a clinical trial. Complion's customers save over $6,000 per trial because staff members spend less time chasing down paper, and physical materials and storage space are no longer needed. Complion has been accessed by more Sponsors and CROs than any other eRegulatory platform.
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