AI-enabled Electronic Data Capture (EDC) System in clinical trials

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Clinion EDC is a powerful electronic data capture system to accelerate study startup and improve data quality. Experience the power of acceleration today!

Clinion Electronic Data Capture Software Making Clinical Trials Faster and Better.

EDC system in clinical trials

The EDC System That Covers Your Entire Clinical Data Management Needs

eCRF Configuration: Our platform offers an intuitive eCRF configuration feature that allows users to create electronic Case Report Forms (eCRFs) effortlessly. You can either start from scratch using the drag-and-drop functionality or choose from a range of customizable forms available in the Global Library.

Study Administration: With our robust study administration module, administrators have the power to efficiently manage various aspects of their studies. This includes overseeing users, sites, roles, medical dictionaries, and all other administration activities.

Local Labs Management: Our system enables you to set up both local and global labs specific to your study and site requirements. You can easily manage multiple lab ranges across different CRFs and sites, streamlining your lab-related processes.

Role-Based Access Control: Clinion's Role-Based Access Control (RBAC) feature empowers you to handle user management and permissions directly from a central interface. This eliminates the need to contact Clinion support for routine user administration tasks, enhancing efficiency and control.

Data Capture: Our platform offers a comprehensive and user-friendly data capture module. It consists of color-coded CRF forms, validations, skip logics, role-based access controls, investigator verification, and more. These features ensure accurate and efficient data collection throughout the study.

External Data Loader: Effortlessly load data from various external sources directly into the system with our external data loader. This feature allows you to run batch edit checks, ensuring data integrity and consistency.

Visit Scheduler: Streamline your study visits by utilizing our visit scheduler. Easily schedule visits for each subject from the date of enrollment to the final visit. Furthermore, you can manage and track visit protocol deviations, ensuring adherence to the study protocol.

CRF Versioning: Maintain multiple versions of your CRF throughout the study or on a site-specific basis. With our CRF versioning feature, you can manage CRF access for both old and new users, ensuring data continuity and control.

Data Extraction: Generate a wide range of ready-to-use reports in XLS and SAS formats. Our platform allows for easy data extraction, enabling you to analyze and interpret study data effectively.

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