mEDC is a comprehensive, yet highly configurable electronic data capture application. It’s a web-based system for managing single or multi-site clinical research studies with complete audit trail. The architecture provides a secure, robust and extensible system for managing multiple clinical research studies within a centralized database.
mEDC provides electronic capturing, cleaning, coding and reporting CRF data, along with other study data in a single system. With the advanced technology, electronic CRFs can be dynamically generated which greatly simplifies and accelerates the entire study process. Based on various user roles, mEDC provides unsurpassed flexibility to protect study data from unintended view or alterations.
Key Features:
Core CDMS functionalities: Study design & Set-up, Edit checks, Auto coding, Discrepancy management, Database Lock, Archival
Single/ Multi-site management
Graphical representation of subject wise data entry status
21 CFR Part 11 compliance with complete Audit trail and Electronic signature
Supports univariate and multivariate edit checks
Supports hybrid studies (both paper CRF and eCRF)
Single/ Double data entry
Intuitive role-based views and displays
Data exports to SAS, CDISC, Excel formats
English and Japanese language support
Key Benefits:
Easy eCRF creation
Reusable CRFs
Easy-to-use interface
Quick deployment and 24/7 support
Minimal training required
Seamless integration with other systems
Faster access to clean data for better decision making
