The Freedom And Flexibility To Built
Studies On Your Own
Integrate Clinion Electronic Data Capture with CTMS, IWRS/RTSM, and ePRO/eCOA for true end-to-end support of your Study, obviating the hassles of data reconciliation while dealing with multiple eClinical solutions.
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.
Clinion EDC Software uses AI and Automation to simplify Study Build, Data Capture and Clinical Data Management(CDM). With advanced features like Medical Coding, External Data Load, Visit Scheduling, Bulk locks, CRF versioning as part of a standard package Clinion makes things simpler for its users.
Clinion's EDC Software is an intuitive tool that simplifies data management and allows easier study setup, data capture, processing, and integration. Users can quickly build and manage clinical studies on their own with our Electronic Data Capture Software.
Clinion EDC Software is easy to sign up and use. Pay for only as much as you use and no more. All of Clinion EDC features are available for a single price.
Users can create an eCRF from scratch by simply using the drag and drop feature or selecting a customisable form from the Global Library.
A powerful study administration module allowing admins to manage studies, users, sites, roles, medical dictionaries and all other administration activities.
Set up local and global labs for your study site-wise. Manage multiple lab ranges across CRFs and sites.
Clinion’s Role based access control allows you to manage users and permissions from a central interface without having to contact Clinion support for any user administration
Comprehensive and user friendly data capture module consisting of color coded CRF forms, validations, Skip Logics, Role based access, Investigator Verification etc.
Load data from various external sources directly into the system and run batch edit checks
Schedule your study visits for every subject from the date of enrolment to the final visit. Manage and track visit protocol deviations.
Maintain multiple versions of your CRF during the Study or site-specific. Manage CRF access for old and new users
A large number of ready reports can be extracted into XLS and SAS formats.
Comprehensive audit and activity logs capture every aspect of system access, data entry and change.
Flexible Source Data verification, locks, data querying, data extraction, external data loading, etc., are some of the features making the work of Data Management easy.
Ad hoc reporting engine allows users to design their own reports and save and import them into XLS and SAS formats.
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