A patented, flexible eClinical ecosystem to give you full command over mission-critical, time-sensitive, and deeply-human interactions.
Clinical trials are becoming increasingly complex, and the pressures to complete them faster are intensifying. Purpose-built trial management technologies are an essential tool to manage through complexity efficiently. Sponsors, sites, and patients need systems that work together seamlessly, integrate easily with other tools, can be updated with precision, and are efficiently deployed.
While others chase just the simplification of trial processes, our approach sees that as only a starting point. That’s why, with the Suvoda Platform, we don’t just bring together all our software products—and their associated data streams—we’ve purpose-built them as part of a dynamic ecosystem that harmonizes the complex interdependencies across their features and functions. The result? The right user is thoughtfully engaged, at the right moment, with the information and insights they need to calmly take the right next step, in the right product. So sponsors, sites, and patients alike feel empowered to take command over the most urgent moments in their journey through a trial.
Our platform delivers:
- Seamless user experience across eConsent, IRT, and eCOA
- A single, robust data model for improved data workflow and reduced integrations
- Customer trial standardization and updates without disruption
- Rapid deployment, even for trials with high levels of protocol, operational, logistical, technical, or cultural complexity
Three clinical trial products built on one platform minimizes friction and maximizes engagement across the user experience for sponsors, CROs, sites, and patients.
Suvoda products—eConsent, IRT, and eCOA—operate on a single patented software platform with a single, robust data model. That means products are fully integrated from the outset. The Suvoda Platform ensures that interactions and data from one product can automatically direct and drive sponsors, sites, and patients to take required actions in another. Because it’s our goal to not just simplify, but actually enhance the experience and contributions of all users across the clinical trial journey.
Platform features:
- Fully integrated product suite with shared user interface across eConsent, IRT, and eCOA
- Single sign on
- Automatic gatekeeping or triggering of activities from one product to another
- User workflow moves smoothly from one tool to the next, without having to switch systems
Patented software design reduces and simplifies integrations, enabling a more robust eClinical ecosystem.
The Suvoda Platform uses best practice software design approaches, recognized with a US patent, to eliminate integration across our three products - and the comprehensive API surface simplifies integrations with other third-party solutions and sponsor systems. Central data management gives you real-time access to information and confidence that your clinical trial data is secure. One system to let you focus on your trial.
Platform features:
- API surface allows seamless integration with your in-house systems and other third-party clinical technologies
- A single, central, and synchronous patient, drug, and site data model across eConsent, IRT, and eCOA
Elegant software architecture means your clinical trial technology will always be current.
Applying the proven strengths of B2B and consumer technology, Suvoda protects and leverages your eClinical investment with a platform designed to remember your standards and keep your trials up-to-date throughout the course of the study. That means your trial software is built on what you have done before and can be upgraded to take advantage of the latest advances in trial technology and functionality. Another way to think about it? Future-proofed eClinical programs.
Platform features:
- Enhanced flexibility makes mid-study changes and protocol amendments less disruptive
- Options to upgrade your system (or opt-out, if you prefer) when updates become available, without losing any customizations
- The Virtual Partition - advanced architecture enables advanced customization and stores enterprise standards to easily apply to future trials
Simplify clinical trial software set up with a harmonized deployment process, a single project team, and low-code/no-code technology.
Clinical trials today are longer than they ever have been and every day counts. Your single Suvoda project team and streamlined deployment across all three products simplifies your overall implementation. The platform allows you to deploy your trial technologies more efficiently and accurately - with low-code/no-code and advanced design tools to power efficient build, deployment, and modification timelines. Even for trials facing high levels of complexity due to unique protocol, operational, logistical, technical, or cultural requirements.
Platform features:
- Harmonized deployment process for all three solutions saves study teams time and effort
- Suvoda XD – a proprietary low-code/no-code toolset - streamlines start-up and mid-study changes and improves service delivery
- The Virtual Partition makes customizations and customer standards easy to implement, for more control over the increasing complexity of today’s trial designs
Elegant user experience, efficient deployment, customizations, and data integrity delivered through patented software architecture.
Suvoda’s clinical trial software architecture leverages the best of B2B and consumer technology platforms, and our unique architectural approach was recognized with a US patent. It delivers the intuitive user experience and efficient set up that people expect out of their technology, while providing the data integrity, customizations, and flexibility needed for clinical trials.
Three essential elements make up the platform architecture:
- The Foundation: building on cloud technology best practices
The Suvoda platform includes a comprehensive API-surface, using the latest cloud technologies. - The Virtual Partition: our patented approach to customizable and upgradable software
A Virtual Partition is built into the software architecture, to allow for trial-specific adjustments outside of the core product code. It allows customization, with benefits of SaaS: upgradability, cloud-based deployment, and a shared data layer. - Suvoda XD - a proprietary low-code/no-code toolset - makes customizations and mid-study changes simpler
The tools allow our teams to:
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- Leverage Suvoda’s library of IRT customizations to expedite implementation timelines and mid-study changes
- Create robust and accurate eCOA questionnaires simply and efficiently manage licensing and localization
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