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Electronic Source Data (e-Source)
GAJA e-Source (Globally Accessible e-Source with Justified Accuracy) is a next-generation solution that enables the direct digital capture of source data at the point of care. It eliminates paper records and duplicate data entry, ensuring accuracy, efficiency, and regulatory compliance in clinical trials.
Why Choose GAJA e-Source for Your Clinical Trials?
- ✔ Paperless & Efficient Streamlines workflows and reduces site burden.
- ✔ Improved Data Accuracy No transcription errors or duplicate entries.
- ✔ Faster Insights Real-time access for sponsors, CROs, and monitors.
- ✔ Regulatory Confidence Fully compliant with 21 CFR Part 11, ICH-GCP standards.
- ✔ Supports Decentralized Trials Enables remote data review and monitoring.
- ✔ Seamless Integration Works perfectly with GAJA EDC, eConsent, eCOA, and RTSM.
Features Of GAJA e-Source
- Direct Data Capture Record data digitally at the point of care.
- Real-Time Synchronization Data instantly available across stakeholders.
- Customizable Templates e-Source forms tailored to study protocols.
- Audit Trails & Security Full traceability of data changes and user activity.
- Remote Monitoring Secure access for off-site monitors and auditors.
- Device & Platform Support Accessible via tablets, mobiles, or desktops.
Benefits of GAJA e-Source
Real-Time Data Capture
Direct entry at the point of care ensures accuracy and instant data availability.
Improved Data Quality
Built-in checks and validations reduce errors and maintain consistency.
Remote Monitoring
Enables sponsors and monitors to review data without frequent site visits.
Audit-Ready Compliance
Maintains complete audit trails to meet FDA, EMA, and GCP requirements.