Suvoda eConsent

Reducing risk, delays, and complexity in the consent process

Informed consent isn’t just the starting point, it’s a recurring, critical step in clinical trials. Most protocols require re-consent after amendments, which can add weeks to timelines and introduce regulatory and operational risk. Suvoda eConsent helps manage this complexity, reducing administrative burden and study costs.

Tools that empower patients—and sponsors

With embedded videos, FAQs, discussion threads, and cross-linked glossaries, the solution supports better patient comprehension of complex trial information. Sponsors gain 100% visibility across all sites and patients, making consent tracking and oversight seamless.

Built for seamless integration and compliance

eConsent is part of the Suvoda Platform. When a consent document is updated, the IRT system automatically checks whether a participant has re-consented. If not, the system prompts completion before allowing the visit to proceed.

A calm, consistent user experience

eConsent shares the same minimalist, intuitive interface as the rest of the Suvoda Platform. This simplifies navigation for study teams and reduces training needs, improving both usability and adoption.

Real-time oversight, better compliance

Consent status is visible in real time via reporting tools. Teams can quickly identify sites or patients pending re-consent, download audit-ready consent archives, and take corrective action early.

Key benefits at a glance:

• Enhance patient understanding: Uses media, FAQs, threads, and glossary tools
• Maintain compliance: 100% visibility into consent and re-consent status across sites
• Simplify workflows: Integrated into IRT to automatically gate visits until consent is current
• Reduce training: Consistent, user-friendly interface
• Enable early intervention: Reporting tools surface consent delays before they become problematic