Clinion EDC logo

Clinion EDC

by Cmed Technology · Since 2010
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Active1+ countriesCloudOn-premise
Quick facts
VendorCmed Technology
Year launched2010
StatusActive
Location5900 Balcones Drive, STE 100, Austin, TX 78731, United States.
Countries served1+
Languages8
Integrations3+
Free tierN/A
Free trialN/A
Contact salesYES

About Clinion EDC

Clinion EDC is an electronic data capture software from Cmed Technology that facilitates the collection and management of clinical trial data. It provides features such as real-time data entry, customizable electronic case report forms, and advanced data validation tools so researchers can efficiently manage their clinical data. Additionally, Clinion EDC supports integration with other clinical trial management systems and offers comprehensive reporting capabilities. It is designed to help ensure data accuracy and compliance with regulatory standards. Key capabilities: real-time data entry customizable electronic forms advanced data validation integration with other systems comprehensive reporting Best for: clinical researchers and trial managers that need to collect and manage clinical trial data effectively.

Clinion EDC is an award-winning, AI-powered Electronic Data Capture (EDC) software that redefines the way clinical trials are managed by integrating automation, intelligent modules, and seamless interoperability. Built to simplify study setup, accelerate trial timelines, and enhance compliance, Clinion provides a flexible and intuitive platform that allows sponsors, CROs, and research sites to streamline every aspect of their clinical data management. By leveraging advanced AI and machine learning, Clinion ensures greater data accuracy, improved efficiency, and reduced costs, making it a trusted solution for modern clinical research. One of Clinion EDC’s standout strengths is its rapid study start-up capability. Unlike traditional systems that take weeks, Clinion allows teams to set up studies within days using its drag-and-drop global library of customizable forms. The platform also automates key processes such as CDASH mapping, data verification, medical coding, and reporting, significantly reducing manual effort. This automation translates into fewer errors, quicker database lock, and improved trial oversight—helping research organizations remain agile in fast-moving clinical environments.

Pros & Cons

Pros
  • Easy to use and efficient for clinical trials
  • Strong support team with quick issue resolution
  • Fast setup and smooth implementation
  • Integrated IWRS with CDMS and real-time alerts
  • Reliable for long-term use (2+ years by many users)
  • Good for data management and biometrics in research
  • Widely recommended by users in pharma and research
Cons
  • Performance and functionalities could be enhanced further
  • Needs benchmarking against leading market products

Features

Key features

AI-Powered Study Setup – Rapid deployment with drag-and-drop tools and CDASH mapping for faster trial initiation.
Global Library & eCRF Configuration – Prebuilt customizable forms reduce programming needs and ensure compliance.
AI Medical Coding – Automates coding of adverse events and medications using MedDRA and WHODD dictionaries.
Remote SDV & Data Review – AI-enabled source data verification reduces on-site monitoring costs and errors.
Labs & Visit Scheduler – Manage multiple lab ranges and schedule patient visits with precision.
Advanced Reporting Engine – Customizable ad hoc reports in multiple formats (CSV, XLS, PDF).
Seamless Integrations – Directly connects with CTMS, RTSM, ePRO, eSource, and eConsent for end-to-end trial management.

Additional features

eCRF Configuration – Drag-and-drop form builder with CDASH coding support.
Study Administration – Manage sites, roles, dictionaries, and administrative functions centrally.
Labs Management – Configure local/global labs with multiple ranges per site.
Visit Scheduler – Organize patient visits and track protocol adherence.
Data Capture – User-friendly interface with validations, skip logic, and investigator verification.
External Data Loader – Import and validate datasets from multiple sources seamlessly.
CRF Versioning – Maintain multiple CRF versions and manage access at the study or site level.
Data Extraction – CDISC-compliant data exports in multiple formats.
AI-Powered Data Management – Includes query automation, bulk closures, and chatbot assistance.
Audit Logs & Compliance – Maintain full transparency with traceable activity logs.

Pricing

Free trial
Free version
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Countries & Languages

1
Countries served
8
Interface languages
13
Billing currencies

Available in

All Countries.

Interface languages

EnglishSpanishFrenchGermanItalianPortugueseJapaneseChinese.

Billing currencies

🇺🇸USD🇬🇧GBP🇪🇺EUR🇯🇵JPY🇦🇺AUD🇨🇦CAD🇨🇭CHF🇨🇳CNY🇸🇪SEK🇳🇿NZD🇰🇷KRW🇸🇬SGD🇭🇰HKD

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