Primesoft’s ez-EDC application incorporates streamlined study design, workflow, query management, regulatory compliance, and extensive reporting and analysis into an integrated solution.

The intuitive interface and streamlined workflow benefit the clinical research coordinators, trial monitors, clinical data managers and project managers to work more efficiently and with greater accuracy. ez-EDC’s advanced reporting and analysis tools are designed to enable sponsors to view and act on data earlier in the trial development cycle and manage studies more effectively.

Integration of the ez-EDC with our other clinical products like ez-SourceDocx for managing source data at the site, ez-DIMS for randomization and drug/device inventory supply management and ez-CTMS for managing study and related budget offers the user a comprehensive electronic clinical data management solution for clinical research.

Key features of ez-EDC are:
  • User-based workflow interface to maximize efficiency
  • Streamlined workflow management
  • Extensive query and discrepancy resolution management
  • Standard-and user-driven reporting for real-time data visibility
  • Designed and developed to support trials of all types and sizes
  • Study design and setup through regulatory submission
  • Complete integration with our products such as ez-CTMS, ez-SourceDocx and ez-DIMS
  • Provides comprehensive electronic clinical data management solution
Delivery and Support
  • Service staff with extensive domain experience available to meet support requirements 24×7
Standards and Industry Regulations
  • CDISC standards compliance
  • Compliance with GCP, Title 21 CFR Part 11 and other regulatory requirements