Site Technology
eSource + EDC
Built for research sites and site networks, workflows within Advarra’s eSource + EDC platform allows you to easily capture and manage data, facilitate remote workflows, and eliminate duplicative processes for your staff.
eSource Capabilities
- Streamlined remote workflows
- Seamless integrations
- Easy oversight and compliance
- Rapid implementation
21 CFR Part 11-compliant eSource
Simplify Data Capture Workflows and Ensure Part 11 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.
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.
Streamline the Part 11 Validation Process
We’re committed to setting up our customers for success in the highly regulated clinical research environment. Our staff and resources ensure rapid time to value through implementation, integration setup, validation, and migration to establish a centralized source for your data and documents.
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.
