Site Solutions

eSource

Electronic Source Data (eSource)

Built for site networks and research sites, Advarra eSource simplifies the transfer of data to any sponsor electronic data capture (EDC) system, eliminating the need for duplicate data entry. Intuitive, easy-to-use, quality-controlled workflows within eSource also help investigators work more efficiently and compliantly.

Learn more about Advarra eSource

Accelerate your research compliance

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

Easily and securely set up remote monitoring sessions for sponsors and monitors. Advarra’s eSource simplifies remote monitoring, allowing you to reduce onsite monitoring costs and more easily support sponsors.

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 your Clinical Conductor or OnCore CTMS.

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.

Integrate with Clinical Conductor CTMS

Seamlessly exchange study and patient information between eSource + EDC and Clinical Conductor. Boost staff efficiency and data quality by automatically sending completed eSource forms to initiate billing workflows in Clinical Conductor, ensuring visits are billed promptly and accurately.

Improving Staff Efficiency with eSource Integration

Taryn Collett, Chief Operating Officer at Tekton Research, shares that integrating eSource within Clinical Conductor eliminates inefficiencies of using separate systems for CTMS and source documentation. This integration streamlines workflows, reduces redundancy, saves time, and improves clarity for site staff.

“The system has helped us improve our data collection processes and helped to make communication more effective. The different options for building form constraints has helped us to ensure higher data quality.”

Courtney Kennedy DNP, RN-BC Manager, Clinical Trials Applications, University of Nebraska Medical Center

Benefit from community knowledge

This 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 heard while shaping the future of your technology.

fEATURED CONTENT

Advarra EDC Validation Packet

Advarra EDC Validation Packet

Reduce the burden of testing and documentation with precompiled validation materials, available through an annual subscription.

Beginner’s Guide to Compliant Electronic Source Data Capture

Beginner’s Guide to Compliant Electronic Source Data Capture

While electronic source data collection is not new, collecting source data in a variety of settings in a compliant manner is. With this in mind, how does one maintain data quality and integrity while ensuring participant safety and staying compliant?

Beginner’s Guide to an Electronic Data Capture (EDC) Systems

Beginner’s Guide to an Electronic Data Capture (EDC) Systems

This post walks you through the basics of an electronic data capture system, providing a high-level overview of benefits and common functionality.

A purpose-built clinical research cloud platform

Built upon clinical research best practices, Advarra Cloud is a next-generation platform delivering applications in an easy-to-use, fully managed environment. Learn how the Cloud can help you automate, connect, and expedite processes across the clinical trial lifecycle.

A purpose-built clinical research cloud platform

Built upon clinical research best practices, Advarra Cloud is a next-generation platform delivering applications in an easy-to-use, fully managed environment. Learn how the Cloud can help you automate, connect, and expedite processes across the clinical trial lifecycle.