SimpleTrials CTMS Integrates with Medrio EDC!
Accelerate Study Oversight with Seamless EDC-CTMS Integration for Tracking, Forecasting & Compliance
The integration between Medrio EDC and SimpleTrials CTMS/eTMF empowers clinical research teams to streamline operations, reduce manual work, and improve oversight across the trial lifecycle. With subject and site data flowing directly from Medrio into SimpleTrials, sponsors and CROs gain immediate access to enrollment metrics, protocol deviations, milestone tracking, and Key Risk Indicators (KRIs)—all within a centralized, cloud-based CTMS.
Whether you're managing early-phase studies or late-stage pivotal trials, the Medrio-SimpleTrials integration delivers the automation and visibility needed to move faster, stay compliant, and scale efficiently.
Why Integrate Medrio EDC with SimpleTrials CTMS?
Medrio’s agile EDC is known for its ease of use and speed. Combined with SimpleTrials CTMS, the result is a unified platform that brings together clinical data and operational workflows. This powerful integration eliminates data silos, reduces duplication, and enables your team to act on real-time insights that improve trial performance and readiness.
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 Medrio EDC to SimpleTrials, enabling proactive risk monitoring and improving inspection 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 Medrio EDC 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 + Medrio EDC
See how your team can benefit from Medrio EDC integration with SimpleTrials.
👉 Book a Demo today!