Join us at SCDM 2025 in Brussels, Belgium. Our experts will be ready to share details on the Suvoda Platform, and show you how our flexible eClinical ecosystem creates a seamless experience across eConsent, IRT, eCOA, and ePatient. Stop by Booth #3 to learn more.
Click here to schedule a demo or on-site meeting at the booth.
Want to learn more? Attend our product showcase:
Presentation
Thursday, April 10th | 3:00pm CET | Room: Aquarium
Streamline Clinical Trial Data Management with a Unified Technology Platform: eConsent, IRT, eCOA, and ePatient
Join us for a demonstration of the Suvoda Platform – purpose-built to seamlessly unify eConsent, IRT, eCOA, and ePatient and to give sponsors and sites complete control over critical and time-sensitive patient interactions.
The Suvoda Platform delivers:
- A common data layer that minimizes human and data synchronization errors and results in greater data integrity
- Real-time exchange and collection of accurate patient, drug, and site data for high-quality study submissions
- An easy-to-use, intuitive user experience
- Improved data visibility for proactive compliance monitoring and resolution during the trial
Speaker: Daniela Duffett, Senior Solutions Consultant | Suvoda