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.
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:
Real-Time ePRO Data Collection
BYOD and Provisioned Device Support
Photo and Video Capture
Automated Reminders and Notifications
Compliance-Driven Participant Engagement
Implementation Expertise & Support
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™
How Smaller Clinical Trials Can Use ePRO Effectively Without Adding Cost or Complexity
Discover how smaller trials can benefit from ePRO technology without increasing operational burden or budgets.
SDC Capture™ Fact Sheet
Get a complete overview of platform capabilities, deployment options, compliance standards, and technical specifications.
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.
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