This year, Suvoda will be at ACDM24, one of the largest clinical data management conferences in Europe. Our experts will be at Booth #16, ready to share more details on the Suvoda Platform, and show you how our flexible eClinical ecosystem creates a seamless experience across eConsent, IRT and eCOA.
Want to learn more? Join our demo sessions!
Full Demo Session
Monday, March 6th | 9:15am
Location: Norway meeting room
Empowered Data Management: Unified Platform for Seamless Data Collection and Real-Time Insights
Join Suvoda as we demonstrate the power of a single clinical trial technology platform that creates a seamless experience across eConsent, IRT, and eCOA. The Suvoda Platform is designed to give sponsors and sites control over critical and time-sensitive patient interactions. In this session, you will learn how this unified approach streamlines trial operations, delivers real-time insights, and maximizes efficiency in data collection and management, especially in complex scenarios.
Here's a preview of what you can expect:
- Discover how the Suvoda Platform facilitates seamless, electronic reporting of outcomes data for patients and site staff and minimizes friction from consent through data submission
- Learn how eCOA data can be leveraged in the IRT to manage inclusion and exclusion criteria
- Witness how the Suvoda eCOA app enables patients to report data remotely and in real-time, promoting patient engagement
- Explore the variety of standard and customizable reports that enhance data visibility and enable proactive compliance monitoring and issue resolution
Bite Size Demo Session
Monday, March 6 | 1:40pm
Location: Denmark meeting room
Streamline Clinical Trial Data Management with a Unified Technology Platform: eConsent, IRT, and eCOA
Join us for a demonstration of the Suvoda Platform – purpose-built to seamlessly unify eConsent, IRT, and eCOA and to give sponsors and sites complete control over critical and time-sensitive patient interactions. During this session, you'll see how Suvoda's practical innovation philosophy puts users at the center, resulting in technology solutions that elegantly solve problems, address current needs, and anticipate future challenges.
- An easy-to-use, intuitive user experience
- Enhanced data workflow and reduced integrations
- Real-time exchange and collection of accurate patient data for high-quality study submissions
- Improved data visibility for proactive compliance monitoring and resolution during the trial