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SDC Capture™ e-PRO/e-COA Platform

Flexible, Cost-Effective ePRO Technology for Clinical Trials

Deploy a flexible, 21 CFR Part 11-compliant ePRO/eCOA solution faster. SDC Capture™ empowers clinical teams to leverage BYOD technology, capture patient data in real time, enhance compliance, and reduce overall trial costs.

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SDC Capture™ Features

Flexible ePRO Technology Designed for Your Trial

SDC Capture™ is a pre-validated ePRO/eCOA platform that enables rapid study deployment through configuration, not custom development. Sponsors and CROs can streamline patient-reported outcome collection, reduce costs, and improve participant engagement. Built to support both bring-your-own-device (BYOD) and provisioned device models, SDC Capture adapts to your protocol, timelines, and budget without compromising data quality or compliance


SDC Capture™ is designed to fit your protocol—not the other way around.

Our configurable platform supports:


Why Sponsors Choose SDC Capture™

SDC Capture™ is purpose-built for studies that need a cost-effective, rapidly deployable ePRO solution—making it an ideal choice for trials with smaller patient populations, shorter timelines, streamlined assessment requirements, and budget-conscious programs.

Reduce Trial Costs

Eliminate expensive paper-based workflows and lower hardware and logistics costs with a BYOD-first approach, delivering a more scalable and cost-efficient ePRO experience.

Improve Patient Engagement

A patient-tested, intuitive user experience reduces participant burden and supports stronger recruitment, retention, and compliance throughout the study.

Enhance Data Quality

Real-time alerts, validation checks, and feedback mechanisms help improve the completeness and accuracy of patient-reported data.

Accelerate Study Timelines

Digital data capture eliminates manual transcription and paper handling, allowing teams to move faster from collection to analysis.

Increase Operational Flexibility

Support diverse patient populations with the ability to use participant-owned or provisioned devices based on study needs and participant preferences.

Ensure Regulatory Compliance

Operate confidently with a fully validated platform designed to meet 21 CFR Part 11 requirements and industry best practices.

With real-time data collection, configurable workflows, and industry-leading support, SDC Capture™ empowers better clinical decisions through a more connected patient experience.

Learn More About SDC Capture™

EMPOWER YOUR CLINICAL DECISIONS

Ready to Streamline Clinical Data Collection with SDC Capture™?

Empower better clinical decisions with a flexible, cost-effective ePRO platform that improves patient engagement, enhances data quality, and accelerates study delivery.