Product Overview
Delivering high-quality patient data with patented technology, rapid deployment, and expert guidance
Collecting quality data on patient outcomes is often one of the most important parts of a clinical trial. It is also challenging, and many eCOA solutions make it feel even more difficult with complicated processes, lack of questionnaire reusability, slow set up, and difficult to use tech.
Suvoda eCOA, coupled with our expert scientific and operational guidance and streamlined licensing and localization, relies on our patented software architecture to solve those problems so teams and implementations are more efficient, especially in the most urgent moments. Suvoda eCOA supports sponsors and CROs to:
- Accelerate eCOA questionnaire creation and deployment, taking eCOA off the critical path so trials can launch more efficiently
- Minimize the many stresses that plague traditional eCOA solutions and delivery
- Streamline the collection of accurate patient data for high-quality study submissions
- Empower sites to focus more time on patients
Sponsors can partner with Suvoda’s scientific advisors and licensing experts to guide eCOA implementation. Site teams will find the complex logistics of getting the right questionnaires to the right patient at the right time are easily and securely managed—just like the drug supply in our IRT system. And just like IRT and eConsent, Suvoda eCOA is supported by our intuitive user experience, standard and ad-hoc reporting, and customer support.
Deployment
- Web based
- Cloud Hosted
Pricing
- Subscription
- License Fee
More Information
To your study and site users, Suvoda eCOA and IRT administration activities will appear in a single unified interface. Why? To simplify your day to day. You can be more efficient with data that is seamlessly shared, streamlined workflows, and a process that is completely controlled. Suvoda eCOA set up is done easily when the IRT functionality is used during a patient’s first study visit. Our shared application logic across eCOA and IRT will enable accurate and complete data collection. And site users can proactively monitor patient compliance in real-time.
About the company
Suvoda is a global clinical trial technology company dedicated to supporting complex studies for life-sustaining therapies. Seamlessly manage mission-critical, time-sensitive, and deeply-human interactions with the Suvoda Platform—a purpose-built, easy-to-use ecosystem delivering eConsent, IRT, eCOA, and ePatient.
Set up your clinical trial technology exactly as your study needs it, with simplified integrations, tools to remember your trial standards, and rapid deployment. Once launched, you’ll find the Suvoda Platform enhances the experience of moving through a study, for your team, your site professionals, and your patients alike. So everyone can confidently contribute to their clinical trial more easily than ever.
