SITE TECHNOLOGY
eSource
Electronic Source Data (eSource)
Built for research sites and site networks, Advarra’s eSource allows your organization to easily capture and manage data, facilitate remote workflows, and eliminate the need for paper source documents or duplicative burdensome processes for your staff. With eSource, you cam streamline data management and 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 system.
Consolidated Data Capture and Management
An integrated eSource platform for sites and site networks with a full-featured site EDC for large sites conducting investigator-initiated trials (IITs).
- Allows for integration with your clinical trial management system (CTMS) and electronic medical record
- Includes a full-featured site EDC for large sites conducting investigator-initiated trials (IITs)
- Supports intuitive, quality-controlled data capture workflows and comprehensive remote monitoring capabilities for easy site-sponsor collaboration
- Streamlines data management and simplifies form building and data collection
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.
Ensure Investigator Oversight
The system is designed to make it easy for investigators to find and follow up on common oversight tasks, such as adverse events and lab results. They can then apply a Part 11-compliant signature to confirm oversight.
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.
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.
