Clinion
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With best-in-class study setup, easy to use interface and technology, Clinion EDC enables you to capture, cleanse, manage and report clinical data for more efficient trial execution. Clinion EDC provides the flexibility to build your entire study from scratch or from a pre-existing global library providing the highest data quality, integrity and security.
Clinion is a global clinical technology company that offers AI-enabled eClinical solutions. ClinionAI consists of EDC, RTSM, CTMS, eCOA, and Document Automation that cover the entire clinical trial lifecycle. Clinion is committed to innovating the future of clinical trials through ClinionAI and empowering its partners to manage trials more efficiently at lesser costs.
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 is a comprehensive solution and is available both as an integrated and stand-alone solution for randomized clinical trials.
ClinionAI uses Deep Learning NLP models to automate the coding of Adverse Events and Concomitant Medication. The AI Medical Coding algorithm has been trained on millions of biomedical terms for medical context learning using machine learning models. MedDRA dictionaries are encoded and embedded in the model. Adverse event terms entered into Clinion EDC are matched with the MedDRA dictionary terms by the ML Algorithm and results with associated confidence scores are displayed. Users can choose the best fit!
Turn your study synopsis into high-quality protocol drafts in record time with the power of Genai. Clinion’s eProtocol Automation uses cutting-edge AI to supercharge protocol drafting, delivering unmatched speed, accuracy, and regulatory compliance. Experience the future of protocol drafting, where 90% of your content is generated automatically in minutes, freeing your team to focus on innovation and excellence.
CSR Automation Clinion’s CSR Automation is built on a native AI foundation, enabling medical writing teams to generate structured, compliant Clinical Study Reports with significantly less manual effort. By extracting content directly from Protocols, SAPs, and TLFs, it ensures consistency, accuracy, and faster turnaround. What can you expect? ● AI-Generated CSR Sections Automatically create structured CSR content by extracting key insights from study documents. ● Built-In Regulatory Compliance Generate reports aligned with ICH E3 guidelines and global regulatory standards. ● Centralized Collaboration and Review Enable teams to review, comment, and refine CSR content with full version control. ● Template-Driven Standardization Use ICH-compliant or custom templates to ensure consistency across all reports. ● End-to-End Version Control Track changes, manage revisions, and maintain a complete audit trail across the CSR lifecycle. Impact Up to 70% of CSR content is auto-generated Up to 70% faster report completion Reduced manual writing effort and review cycles
Clinion ePRO Clinion ePRO is a secure platform designed to capture patient-reported outcomes directly from patients in real time. With support for mobile and web access, it enables seamless data collection while ensuring accuracy, compliance, and patient engagement across studies. What can you expect? ● Integrated or Standalone Deployment Use ePRO as a standalone solution or integrate seamlessly with Clinion EDC for unified data flow ● Direct Patient Data Capture Collect responses directly from patients through mobile or web, eliminating intermediaries and reducing data delays. ● BYOD Flexibility Allow patients to use their own devices, improving participation and reducing operational overhead. ● Real-Time Data Validation Validate responses instantly and sync data securely with Clinion EDC or operate in standalone mode. ● AI-Driven Data Checks Compare ePRO and EDC data to identify discrepancies early and reduce manual queries. ● Multilingual and Configurable Forms Deploy customized questionnaires with support for global studies and licensed instruments. Impact Improved patient compliance through reminders and an easy-to-use interface Reduced manual queries with early discrepancy detection Scalable across single-site and global trials
Clinion eSource Clinion eSource enables site teams to capture clinical data directly at the point of care, reducing manual entry and delays. Built within a unified platform, it ensures accurate, complete, and audit-ready data from the start. What can you expect? ● Direct Data Capture at Source Enter data during patient visits to remove duplicate entry and reduce transcription errors. ● Real-Time Sync with EDC Sync source data directly with Clinion EDC to maintain consistency across systems. ● Faster Study Execution Reduce data cleaning effort and move studies forward with ready-to-use data. ● Reduced Monitoring Effort Enable focused monitoring with real-time visibility into site data. ● Audit-Ready Compliance Maintain full traceability with timestamps and version control aligned with regulations. ● Easy-to-Use Interface Simplify data entry with a clean interface designed for site users. Impact Reduced manual entry and transcription errors Faster database readiness Lower monitoring effort
Agentic AI Assistant Clinion’s Agentic AI Assistant changes how teams interact with clinical trial data. Users can simply ask questions and get instant answers drawn directly from study data, protocol context, and operational workflows, instead of navigating through complex datasets. Powered by a system of specialized agents, it interprets intent, connects it to the right data source, and delivers responses that are grounded, traceable, and ready to use. What can you expect? ● Ask questions, get direct answers Interact with study data, protocol details, and operational metrics using natural language. ● Understands study context Maps questions to protocol structure, CRFs, and metadata to return relevant outputs. ● Specialized agents working in the background Different agents handle protocol logic, clinical data, and operations to ensure accuracy. ● Responses you can trust Every answer is grounded in study data with clear traceability and no cross-study overlap. ● Works inside your EDC Access insights in real time without switching tools or waiting on data teams. ● Ready from day one Automatically builds a study-specific knowledge base as soon as the study is set up. Impact Faster access to answers across teams Reduced reliance on manual data pulls More confident decisions with traceable outputs
Clinion Reviews
Sapna K.
Clinical Data Management Executive at Syngene International Limited
Verified User in Pharmaceuticals
Ravi K.
SAS base and advance fresherAbout
What is Clinion?
Clinion Inc is a forward-thinking clinical trial solutions provider, built on a native AI foundation that powers its integrated eClinical platform. Designed to improve the efficiency of clinical studies, the platform unifies EDC, RTSM, CTMS, eConsent, ePRO, eSource, eProtocol Automation, CSR Automation, and eTMF in a single interface, simplifying trial execution. Clinion enables seamless data flow across the study lifecycle, helping teams reduce manual effort and move studies forward with greater speed and control. With adaptive and scalable capabilities, the platform supports a wide range of trials, from early-phase studies to complex, multi-country programs. Focused on practical innovation, Clinion equips researchers, CROs, and pharmaceutical companies with the tools needed to manage trials efficiently while maintaining data consistency and operational clarity.