Unmatched Innovation, AI-First.

Industry’s Most-Awarded
eClinical Platform
Powered by AI

Integrated. Intuitive. Intelligent

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.

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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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Accelerate protocol generation with GenAI, transforming study synopses into high-quality drafts in minutes. Automate 90% of creation while ensuring 100% ICH M11 compliance. Cut costs and timelines by 60% and enhance collaboration with Human-in-the-Loop validation for accuracy and reliability.

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Clinion EDC is an AI-driven, user-friendly platform for seamless clinical data management. Integrated with Clinion CTMS, RTSM, and eCOA, it simplifies study setup and execution. With features such as medical coding automation, external data load, and visit scheduling, it enables rapid deployment within days, ensuring efficiency, accuracy, and compliance.

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Optimize randomization and trial supply management with Clinion RTSM. Integrated with Clinion EDC, it automates patient randomization, drug allotment, and inventory tracking. Manage site supplies efficiently, ensure real-time stock visibility, and deploy in 2-3 days - cutting costs while maintaining accuracy and compliance.

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Simplify informed consent with Clinion eConsent. Deliver an interactive UX, multimedia-rich forms, and seamless reconsenting with real-time tracking. Improve patient understanding, reduce site burden, and ensure compliance. Supports on-site, remote, and BYOD consent for a seamless, unified data flow across patients, sites, and sponsors.

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Clinion ePRO streamlines clinical data capture with AI automation, multilingual support, and seamless EDC integration. Enable patients to enter data via mobile, tablet, or web with automated reminders to boost compliance. Pre-built forms accelerate setup while ensuring regulatory compliance. Scalable for global trials, supporting high patient volumes.

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Enhance clinical data collection with Clinion eSource for real-time, direct entry at the point of care. Fully integrated with Clinion EDC, it leverages AI to eliminate transcription errors, improve accuracy, and ensure traceability. Built-in validations flag discrepancies instantly, reducing SDV efforts while ensuring human oversight.

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Automate medical coding with Clinion AI for 85%+ accuracy and audit-ready results. Reduce manual effort by 50% with AI-driven coding that understands clinical context, ranks best-fit codes, and integrates seamlessly with your EDC. Ensure speed, compliance, and full traceability while maintaining human oversight.

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Clinion CTMS offers a centralized system for CROs and Sponsors, ensuring full visibility into study progress and trial efficiencies. It streamlines project management, study monitoring, expense tracking, and scheduling. Integrated with Clinion EDC and RTSM, it provides a holistic view of the entire trial for seamless operations.

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Generate high-quality Clinical Study Reports faster with Clinion AI. Automate CSR writing, extract key insights, auto-populate sections, and ensure ICH E3 compliance. Reduce manual effort, eliminate formatting hassles, and cut CSR timelines by 70% while ensuring accuracy and control.

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Clinion eTMF streamlines trial management with pre-built DIA models, real-time tracking, and automated version control. Ensure compliance with audit trails, e-signatures, and secure document management. Advanced analytics, bulk uploads, and intuitive filing simplify TMF oversight, ensuring inspection readiness.