This whitepaper presents insight and expertise on how investigative sites can begin the transformation to digital documents, including concrete, practical suggestions for eliminating the inefficiencies inherent in printing, storing, and managing paper documents. For clinical site staff, educating themselves before the adoption or purchase of regulated content repositories is key to making the best decisions and driving their success, including improved patient experiences.
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. On average, Complion's customers save over $6,000 per trial from improved staff productivity and reduced materials expense. Visit www.complion.com.