Clinion
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Clinion eConsent replaces manual consent processes with a digital system designed to improve patient onboarding and ensure compliance. Built within a unified platform, it enables real-time tracking, secure documentation, and seamless integration with Clinion EDC. What can you expect? ● Flexible Consent Models Support site-based, remote, and ePRO-linked consent workflows based on study needs. ● Faster Patient Enrollment Reduce onboarding timelines with digital consent and automated re-consenting for protocol updates. ● Real-Time Tracking and Oversight Monitor consent status and patient progress with complete visibility. ● ICF Version Control and Audit Trail Track consent versions with time-stamped signatures and maintain compliance-ready records. ● Improved Patient Experience Use multimedia-enabled consent forms to support better understanding and engagement. ● Seamless EDC Integration Automatically enroll subjects and sync consent data directly with Clinion EDC. Impact Faster patient enrollment timelines Reduced paperwork and manual tracking Improved compliance with audit-ready documentation
Clinion eTMF Help teams manage clinical trial documents in a structured way, with real-time tracking and consistent oversight. It reduces the need for manual follow-ups and keeps documentation aligned with study requirements throughout the trial. What can you expect? ● Defined TMF Structure Set up file plans using standard or custom structures across study, country, and site levels. ● Real-Time Tracking of Documents Track expected documents and identify missing or delayed files as the study progresses. ● Controlled Review and Approval Manage document workflows with review, QC, and approval steps, including e-signatures. ● Ongoing Visibility Monitor completeness and status through dashboards without waiting for end-of-study checks. ● Flexible Configuration Adapt the TMF structure and workflows based on study or sponsor requirements. ● Audit-Ready Records Maintain version history and activity logs to support inspections and compliance. Impact Reduced reconciliation effort during closeout Lower manual tracking effort Better visibility into document status
Clinion’s DICOM Image Repository enables clinical teams to upload, de-identify, store, and access medical images within the same system used for trial data. AI is used to automate image processing, helping reduce manual effort while keeping data compliant and traceable. What can you expect? ● AI-Based Image De-Identification Automatically detect and remove patient identifiers from images in under 30 seconds before storage. ● Direct Integration with EDC Link images to subject records, visits, and CRF pages to maintain consistency across data. ● Support for Multiple Formats Upload and manage DICOM, JPEG, PNG, and PDF files within a single system. ● Built-In Image Viewing Access and review images using an integrated viewer without external tools. ● Centralized Storage and Access Store images securely and access them through a browser from any location. ● Traceable Audit Records Maintain logs of uploads, changes, and access to support compliance requirements. Impact Image de-identification completed in under 30 seconds Reduced manual handling of imaging data Improved alignment between imaging and clinical data
Clinion's Clinical Trial Management Software (CTMS) gives enhanced visibility into all aspects of the clinical trial process - from study plan, Remote monitoring, and Clinical data management.
Clinion eCOA is an electronic clinical outcome assessment solution consisting of ePRO and eConsent. See how
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.