SimpleTrials + Zelta by Merative EDC Integration!
Real-Time Clinical Trial Oversight with Seamless EDC & CTMS Connectivity
Looking for a modern, connected approach to clinical trial management? The SimpleTrials Clinical Trial Management System (CTMS) now integrates with Zelta by Merative EDC, providing your team with access to operational and subject-level data across all study sites.
Whether you’re a sponsor, CRO, or academic research group, this integration eliminates manual workflows and equips your team with the visibility and insights needed to keep trials on track, on time, and inspection-ready.
Why Integrate Zelta EDC with SimpleTrials CTMS?
Clinical trials require collaboration, visibility, and operational agility. With the SimpleTrials + Zelta EDC integration, your team can track subjects, sites, and risk metrics all from within a single, centralized CTMS platform.
The API-driven integration ensures your EDC and CTMS are always in sync—allowing clinical operations and data management teams to work smarter together.
Benefits of EDC Integration to SimpleTrials CTMS:
Automatic population of Subjects, including: screens, screen failures, enrolled subjects, discontinued subjects, completed subjects, etc. This eliminates the need to manually enter subjects into the CTMS.
Automatic population of Subject Visit progress, including Actual Visit Date and visit status values. This minimizes the data entry required to keep subject visit tracking records up to date.
With subject data automatically populated:
Subject payment tracking records can be automatically generated based on visit date and/or status.
Protocol Deviation Tracking allow users to track protocol deviations directly from Viedoc to SimpleTrials, enabling proactive risk monitoring and improving inspecation readiness.
Study Forecasting leverages synced enrollment data to generate automated projections and timelines across all sites and studies.
Key Risk Indicators (KRIs) monitor operational risk using real-time KRIs such as screen failure rate, enrollment, and deviation trends.
Electronic Visit Reports allow for easier tracking of subject activity for monitoring visits, including subject consent, protocol deviations, adverse events, etc.
Projected subject visit schedule can be automatically generated for each subject record, with the option to display projected visits on the calendar.
Dashboards and analytics show recruitment process, actual vs. target, and more.
How It Works
Our technical team enables secure, study-specific connections between Zelta by Merative and SimpleTrials using robust APIs. Once connected, subject enrollment, site performance, and protocol deviations flow directly into the CTMS for instant visibility and reporting.
SimpleTrials: Affordable, Scalable, and On-Demand
Whether you're managing a single study or an entire portfolio, SimpleTrials offers flexible subscription plans that grow with your organization. Our cloud-based, validated CTMS is designed for speed, simplicity, and compliance—perfect for emerging biotechs, CROs, and academic researchers alike.
Get Started with SimpleTrials + Zelta by Merative
See how your team can benefit from Zelta EDC integration with SimpleTrials.
👉 Book a Demo today!