July 23, 2025
Embrace Integration
Integrate EDC software with CTMS, RTSM, eConsent, eSource, and ePRO for seamless end-to-end study support, eliminating the complexities of data reconciliation across multiple eClinical solutions.
Rapid Study Start-Up
Set up your study in days instead of weeks with an easy-to-use interface and a Global Library that doesn't require programming and enables rapid deployment.
Intelligent EDC Software
Clinion’s AI-powered EDC software simplifies study setup, data collection, and overall clinical data management. Automate key steps of your study, including Study Setup, CDASH mapping, Remote Source Data Verification, AI Medical Coding, Data Review, and Custom Reporting, with intelligent modules that work seamlessly together.
Simplifying Data Management
Clinion electronic data capture software is an intuitive tool that simplifies clinical data management and allows easier study setup, data capture, processing, and integration. Users can quickly build and manage studies on their own with our AI-enabled EDC system.
Pay As You Go
Clinion EDC software is easy to set up and simple to use. Pay only for what you use, with all Clinion EDC platform features included at a single price.
The EDC Software That Covers Your Entire Clinical Data Management Needs
Study Setup
- eCRF Configuration
eCRF ConfigurationSelect customizable forms from the Global Library or create eCRFs using the drag-and-drop feature. Apply AI CDASH coding to automatically annotate fields as per CDISC standards.
- Study AdministrationStudy Administration
Manage studies, users, sites, roles, medical dictionaries, and all administrative tasks efficiently with the powerful study administration module.
- Labs ManagementLabs Management
Set up local and global labs for each study site and manage multiple lab ranges across CRFs and sites.
- Visit SchedulerVisit Scheduler
Schedule study visits for every subject, from enrollment to the final visit, and track protocol deviations.
- Data CollectionData Collection
Capture data using a user-friendly module with color-coded CRFs, validations, skip logic, role-based access, and investigator verification.
- External Data LoaderExternal Data Loader
Import data from multiple external sources directly into the system and run batch edit checks seamlessly.
- Data integrationData integration
Integrate Clinion EDC software with ePRO, eSource, RTSM, CTMS, and eConsent for smooth, centralized data management.
- CRF VersioningCRF Versioning
Maintain multiple CRF versions during the study or site-specific settings, managing access for new and existing users.
- Data ExtractionData Extraction
Extract a multitude of ready reports from Clinion, all CDISC-compliant with simplified data transformation and standard processes. Choose from CSV, XLS, or PDF formats.
- AI Medical CodingAI Medical Coding
Automate coding of Adverse Events and Concomitant Medications using Clinion AI with MedDRA and WHODD dictionaries.
- Data ManagementData Management
Simplify clinical data management with AI-powered Remote SDV, automated data review, auto-generated queries, bulk query closure, and 24/7 chatbot support.
- Reporting EngineReporting Engine
Ad hoc reporting engine allows users to design their own reports and save and import them into multiple formats.
Bring Your Entire Study On One Platform!
Find Out How Clinion EDC Software Can Help You
Frequently Asked Questions (FAQ)
What are the key features to look for in an electronic data capture software?
Key EDC features include:
- Intuitive eCRF Design: Simplifies data entry, reducing errors.
- Real-Time Edit Checks: Flags errors instantly.
- Audit Trails: Ensures regulatory compliance (e.g., 21 CFR Part 11).
- Role-Based Access: Secures data with permissions.
- Integration: Connects with CTMS, RTSM, and ePRO.
- Protocol Flexibility: Adapts to changes.
These features, combined with AI-driven automation and an intuitive user interface, create a seamless clinical trial management system.
How does Clinion EDC ensure data security and regulatory compliance?
Clinion EDC ensures robust data security and regulatory compliance by adhering to global standards, including ISO certifications, EU Annex 11, ICH-GCP, GDPR, and 21 CFR Part 11. It safeguards sensitive clinical trial data through advanced encryption, role-based access controls, and comprehensive audit trails that track all system changes.
What are the main advantages of using Clinion AI-enabled EDC Software?
Clinion AI-powered EDC accelerates clinical trials and cuts costs by automating time-consuming manual tasks. It streamlines reporting, simplifies data review, and speeds up medical coding, enabling faster, higher-quality data delivery. This leads to smoother execution and significantly shorter trial timelines.
What integration capabilities do modern EDC systems offer in clinical trials?
Modern EDC systems are built to integrate with clinical tools such as CTMS, RTSM, and ePRO platforms. These integrations support real-time data flow, eliminate silos, and streamline trial execution, reducing manual effort and improving efficiency. For example, Clinion offers an advanced EDC solution that seamlessly integrates with these systems to deliver a unified, high-performing clinical trial environment.
How does Clinion EDC compare to other existing EDC systems for clinical data management?
Clinion EDC offers a competitive edge over many existing EDC systems, particularly for small to mid-sized clinical trials. Its user-friendly and affordable platform simplifies trial setup, with AI-powered features like medical coding and query resolution that cut implementation time to just a few days and help reduce data errors by up to 30%. While many traditional systems involve lengthy and complex configurations, Clinion provides a more agile solution, with features that can adapt to the growing needs of your trial processes.
