Reduce Audit Findings While Increasing the Quality of Your Consent Process

Advarra eConsent is an electronic consenting module for research sites, designed to keep participants engaged, simplify compliance oversight, and optimize the overall quality of the consenting process.

About eConsent

Advarra eConsent helps your site reduce audit risk and keep participants engaged, while tracking consenting progress across your portfolio. By simplifying this process for staff with detailed analytics, remote access, and real-time alerts, sites gain significant improvements in consenting efficiency and a boost in informed consent form (ICF) data quality. eConsent is available as a module within Advarra’s eRegulatory Management System.

Why eConsent?

Boost Participant Engagement

• Ease participants through steps
• Allow participant device of choice

Enhance Consenting Compliance

• Standardize the eSignature process and maintain HIPAA and 21 CFR Part 11 compliance
• Allow participants to opt-out any time

Ensure Consent Process Efficiency

• Standardize regulatory and personal forms
• Provide audit trails

Increase Participant Enrollment

• Intuitive form templates
• Complete process oversight

Accelerate Consent Processes

• Controlled eSignature workflows
• Simplified remote monitoring

Integrate Across Your Organization

• Ensure your team is using the most up-to-date ICF by integrating with Advarra’s CIRBI platform
• Easily populate protocol information with OnCore and Clinical Conductor interfaces