EDC
About EDC
The Electronic Data Capture (EDC) module is at the core of modern clinical trial management. It simplifies the collection, validation, and management of clinical data by replacing paper-based methods with a secure digital system. Our EDC ensures accuracy, efficiency, and compliance, enabling sponsors, CROs, and research sites to make informed decisions faster. With built-in quality checks and real-time monitoring, the EDC module transforms how trials are conducted—delivering speed, reliability, and regulatory confidence.
Our EDC module is designed to streamline data collection and management at every stage of the trial:
Implementing the EDC module brings measurable advantages to all stakeholders in the clinical trial ecosystem:
Contact us to learn how our EDC module can accelerate your trials with speed and compliance.
📅 Request a Demo or 📥 Download the EDC Brochure to explore how it improves study efficiency.
Is the EDC module compliant with regulatory requirements?
Yes, our EDC is fully compliant with global regulations including FDA 21 CFR Part 11, GDPR, and ICH-GCP.
Can the EDC integrate with other trial management systems?
Absolutely. The module integrates seamlessly with ePRO, RTSM, Tele-Health, and other clinical systems.
How secure is the data stored in the EDC?
All data is encrypted and hosted on secure, cloud-based servers with strict access controls.
Is the system suitable for small as well as large trials?
Yes, the EDC is scalable to meet the needs of both small single-site studies and large global trials.
Does the EDC offer real-time monitoring?
Yes, sponsors and CROs can track progress and data trends with real-time dashboards and reporting tools.