eSource

Our unified platform delivers powerful benefits

• A continuous patient experience.
• Automated workflow reminders/ alerts.
• Real-time data and analytics.
• Ease of remote monitoring with 100% data visibility.

Integrates with any EDC, portals, and other systems

• Modern, extensible architecture with easy-to-use open APIs.
• Custom engineering support from our technical team.
• System integration testing and validation support.

Compliance with regulatory requirements

• HIPAA & GDPR compliant.
• 21 CFR Part 11.
• ICH/GCP.

Direct Data Capture

Including direct entry of clinical data by site staff into a mobile application or EDC system.

Non - CRF

It includes the collection and transfer of data in electronic format from internal sponsor sources or external vendors into clinical research data repositories/warehouses without entering the data on a CRF.

Devices & Apps

It covers the collection and management of clinical data from off-site trial participants and research staff using mobile devices including smartphones or tablets, applications, wearable devices, and sensors.