.webp?width=200&height=52&name=SDC-01%20(1).webp "SDC-01 (1)")
SDC DataHub™
A single source of truth - SDC Datahub unifies all third-party clinical data streams into a single, validated data warehouse — giving every study a clean, auditable foundation.
SDC Insights™ 2.0 with SDC Sidekick AI
SDC Insights provides customizable dashboards, near real-time reporting, and cross-system analytics that help sponsors monitor study performance, identify trends, and make informed decisions faster.
SDC Capture™
A flexible ePRO/eCOA platform designed for modern clinical trials. SDC Capture enables rapid deployment of patient-reported outcome solutions while improving patient engagement, supporting protocol compliance, and simplifying data collection.
EDC & RSTM (IRT and CSM) Technologies
SDC supports implementation, integration, and management of industry-leading Electronic Data Capture (EDC) and Interactive Response Technology (IRT) platforms. Our team helps sponsors select and deploy solutions that optimize data collection, randomization, drug supply management, and study oversight.
Capabilities Include:
- EDC platform selection and implementation
- RTSM/IRT strategy and deployment
- Data integrations across clinical systems
- Study startup and ongoing support
- Global scalability and compliance
Safety & Pharmacovigilance Technologies
Patient safety remains at the center of every clinical trial. SDC integrates best-in-class pharmacovigilance and safety systems that support regulatory compliance, case management, and proactive safety monitoring throughout the development lifecycle.
Capabilities Include:
- Safety database management
- Adverse event and SAE processing
- Regulatory reporting
- Signal detection and monitoring
- Integrated safety analytics
Site eSource Technologies
Modern trials require efficient, accurate, and patient-centric data collection. SDC partners with leading eSource providers to enable direct data capture at the point of care, reducing transcription burden and enhancing data quality.
Benefits Include:
- Improved site efficiency
- Reduced manual data entry
- Enhanced data quality and traceability
- Faster access to study data
- Improved site and patient experience
