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What is Clinion and how does it work?
Clinion is a comprehensive eClinical trial platform for small and midsize CROs, academic research groups, and pharmaceutical corporations. It allows users to handle the intricacies of clinical trials with simplicity by sharing consistent trial data across the entire trial process, resulting in speedier clinical development, increased compliance, and faster time to market. Clinion Electronic Data Capture can be integrated with CTMS, IWRS/RTSM, and ePRO/eCOA for complete end-to-end study assistance, eliminating the headaches of data reconciliation when working with several eClinical systems. Randomization and trial supply management (RTSM) processes are improved with Clinion's RTSM system. Clinion RTS and Clinion EDC are intimately connected, allowing sites to get randomization and kit assignment directly from the EDC. Clinion ePRO is a mobile and web-based solution for patient diaries that is integrated with Clinion EDC. Clinion ePRO can be utilised as a bring-your-own-device (BYOD) solution to improve participant compliance and study data quality while also complying with global regulatory requirements. Moreover, scale down costs and improve productivity by automating study and submission document generation.
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