Optimize your consenting process and reduce audit findings at your site
Advarra’s site eConsent module keeps participants engaged, improves study comprehension, simplifies oversight, and enhances audit readiness.
- Ensuring compliance with consent versioning, signature audit trails, and adherence to 21 CFR Part 11 requirements
- Enabling users to sign consent forms remotely via their own device while leveraging two-factor authentication to ensure security
- Boosting staff efficiency with integrated workflows:
- Approved consent document interface with Advarra’s CIRBI platform
- Protocol integration with OnCore and Clinical Conductor CTMS
- Allowing regulatory and clinical staff to easily track the progress of each participant consent
Request a demo to see how eConsent can help reduce audit findings and increase the quality of your consenting process.
DATE
Time: 1 p.m. ET, 12 p.m. CT, 10 a.m. PT
Duration: 1 hour