Streamline Data Collection, Management, and Compliance

Enable your staff to easily capture and manage data, facilitate remote workflows, and eliminate duplicative processes, all in a 21 CFR Part 11-compliant, integrated eSource + EDC system.

One System, Comprehensive Data Capture and Management

eSource

Advarra eSource + EDC allows your team to capture accurate data in real time, eliminating the need for paper source documents or burdensome digital workflows. The platform includes intuitive, quality-controlled data capture workflows and comprehensive remote monitoring capabilities to allow for easy site-sponsor collaboration.

Electronic Data Capture (EDC)

With purpose-built EDC workflows for sites conducting investigator-initiated trials (IITs), the Advarra eSource + EDC platform streamlines data management and simplifies form building and data collection. And turnkey integrations allow your team to interface with your CTMS and EMR.

Learn More About eSource + EDC

• **Accelerate your research with an efficient, Part 11-compliant platform: **Quickly and easily capture data, while ensuring data security and integrity using audit trails and secure signatures to fully support 21 CFR Part 11 validation and compliance. Advarra offers services to assist validation and materials to ensure validation is maintained throughout each upgrade.
• **Enable site-sponsor collaboration with remote workflows: **Easily and securely set up remote monitoring sessions for sponsors and monitors. Advarra eSource + EDC simplifies remote monitoring, allowing you to reduce onsite monitoring costs and more easily support sponsors.
• **Leverage system interoperability to improve productivity and data quality: **Enable data transfer into the system using our FHIR lab results interface and out of the system using our data export API. Or take advantage of integration with OnCore CTMS to pull information related to organizations, protocols, and subjects. Clinical Conductor CTMS integration coming soon.
• **Benefit from the knowledge of the Onsemble Community: **The system was developed in close collaboration with top research institutions across the globe, ensuring it meets the research community’s needs. Join product collaborations to ensure your voice is being heard, and shape the future of your technology.

Efficiently Implement and Validate your Advarra Technology

Reduce System Validation Burden with Advarra Validation Support

At Advarra, we’re committed to setting up our customers for success in the highly regulated clinical research environment. While the implementing organization is ultimately responsible for validation, we aid your path towards validation within our Part 11-compliant systems. Our approach ensures rapid time to value through implementation, integration setup, validation, and migration to establish a centralized source for your data and documents.