Patented software design reduces and simplifies integrations, creating a more cohesive eClinical ecosystem.

The Suvoda Platform uses best practice software design approaches, recognized with multiple U.S. patents, to eliminate the need for traditional integration across our eight products. The comprehensive API surface simplifies integrations with 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 layer that is shared across the platform

Elegant software architecture means your clinical trial technology will always be current.

Suvoda protects and leverages your eClinical investment with a platform designed to remember your standards and keep your trials up-to-date throughout the study. That means your trial software is built on what you have done before and can be upgraded to the latest trial technology and functionality. Another way to think about it? Future-proofed eClinical programs.

Platform features:

• Flexible architecture makes mid-study changes and protocol amendments less disruptive
• Options to upgrade your system (or opt-out, if preferred) when updates become available, without losing any customizations
• The patented Virtual Partition architecture enables advanced customization and stores enterprise standards to easily apply to future trials

Simplify software set up with streamlined deployment, a single project team, and low-code/no-code technology.

Clinical trials today are longer than ever and every day counts. Your dedicated Suvoda project team and streamlined deployment across all eight products simplifies your overall implementation. The platform allows you to deploy 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 protocol, operational, logistical, technical, or cultural complexities.

Platform features:

• Harmonized deployment process for all eight 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 standards easy to implement, for more control over increasing complexity

Modern user experience, efficient deployment, customizations, and data integrity.

Suvoda’s clinical trial software architecture leverages the best of B2B and consumer technology platforms, and our unique architectural approach has been recognized with multiple U.S. patents. 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:

1. The foundation: building on cloud technology best practices
   The Suvoda platform includes a comprehensive API-surface, using the latest cloud technologies.  
   
   
2. 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.
   
   
3. Modern user experience: efficient deployment, customizations, and data integrity.
   The tools allow our teams to:
• Leverage Suvoda’s library of IRT customizations to expedite implementation timelines and mid-study changes
• Easily create robust and accurate eCOA questionnaires and efficiently manage licensing and localization