Clinion's AI-enabled eClinical platform integrates EDC, RTSM, CTMS, eConsent, ePRO, eSource, eProtocol Automation, CSR Automation, and eTMF to streamline clinical trials. Our advanced AIML and GenAI modules accelerates trial timelines, enhances compliance, and reduce costs, making trial management seamless and efficient.
Experience accelerated development, enhanced compliance, and a faster go to market with our cutting-edge solutions.
Studies
Our Products
EDC
Streamline and accelerate your studies with a best-in-class study setup and an easy-to-use interface. Clinion EDC empowers you to set up, capture, manage, and report clinical trial data seamlessly. Experience a new era of clinical trial data management that's smarter and more accessible with Clinion EDC, all while maintaining the highest standards of data quality, integrity, and security.
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RTSM
Clinion RTSM solution optimizes randomization and trial supply management (RTSM) processes. Clinion RTSM is tightly integrated with Clinion EDC, offering sites both randomization and kit assignment from the EDC directly. Clinion RTSM can manage complex studies and is available both as an integrated and stand-alone solution for randomized clinical trials.
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eCOA
Clinion eCOA is a mobile and web-based solution integrated with Clinion EDC. Clinion eCOA can be set up as a BYOD solution and is designed to improve participant engagement and compliance leading to improved study data quality. Clinion eCOA can be deployed in multiple languages and can be set up in days
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CTMS
Clinion CTMS provides a single, centralized system that delivers greater visibility into study progress and trial efficiencies to CROs and Sponsors. Clinion CTMS provides essential project management, study monitoring, expense management and scheduling tools to completely manage all the operational aspects of a clinical trial.
Clinion CTMS is integrated with Clinion EDC and Clinion RTSM to provide a holistic picture of the entire trial.
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Document Automation
Clinion Document Automation tool automates Study Protocol and Clinical Study Report generation using AI, saving weeks of authoring effort leading to reduced submission timelines and increasing speed to market.
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