What is Clinion and how does it work? Clinion is a comprehensive eClinical trial platform designed for small and midsize CROs, academic research groups, and pharmaceutical corporations. It simplifies the management of clinical trials by allowing users to share consistent trial data throughout the entire trial process. This results in faster clinical development, increased compliance, and quicker time to market. Clinion Electronic Data Capture can be integrated with other systems like CTMS, IWRS/RTSM, and ePRO/eCOA to provide complete study assistance and eliminate the challenges of data reconciliation when using multiple eClinical systems. The RTSM system of Clinion improves the processes of randomization and trial supply management. Clinion RTS and Clinion EDC are closely linked, allowing sites to directly access randomization and kit assignment through the EDC. Clinion ePRO is a mobile and web-based solution for patient diaries, integrated with Clinion EDC. It can be used as a bring-your-own-device (BYOD) solution to enhance participant compliance and study data quality while also meeting global regulatory requirements. Additionally, automating study and submission document generation helps reduce costs and improve productivity.
