Adapting to developments of the COVID‑19 pandemic
Direct-to-patient shipping for hybrid and virtual clinical trials
Built in agility to navigate the unexpected
Rapid startup for complex studies
The Suvoda services team can implement your most complex studies from Requirements to UAT in as little as four weeks with Suvoda’s modular architecture.
With Modularity we can offer you the benefits of both. That and a re-usable module library allows for implementing standards that are future-proof and timelines that work for you, every time.
Working with our previous IRT vendor on our last clinical trial was a real challenge. My team and I have spoken on multiple occasions about how simply changing to Suvoda on our most recent study completely changed our approach and experience in managing the trial.
When running complex clinical trials, you can’t predict the future, and now you don’t need to. Suvoda’s best-in-class functionality allows you to confidently expect the unexpected in your clinical program. Whether you need to add dose levels mid-study or need to dynamically expand cycles in your oncology trial, the Suvoda IRT system helps you gracefully navigate the inevitable unknowns in your trial.
Suvoda Trial Intelligence provides you with insight into your current and historical clinical trial performance. Key data points, KPIs, and trends across multiple trials are presented in a unified interface, letting you make informed decisions to effectively manage a single study or an entire clinical program.
Visualize data and trends within and across trials
Gain insight into trial performance using KPIs, metrics, and trends
Make better, faster decisions to plan and execute your clinical trials