A single clinical trial technology platform

Advanced software design reduces and simplifies integrations, enabling a more robust eClinical ecosystem.

The Suvoda Platform uses best practice software design approaches 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
• Central and synchronous patient, drug, and site data management 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
• Advanced architecture 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 the most complex trials.

Platform features:

• Harmonized deployment process for all three solutions saves study teams time and effort
• Low-code/no-code technology streamlines start-up and mid-study changes and improves service delivery
• Easy-to-implement customizations and customer standards for more control over trial design, especially for complex trials

Elegant user experience, efficient deployment, customizations, and data integrity delivered through cutting-edge software architecture.

Suvoda’s clinical trial software architecture leverages the best of B2B and consumer technology platforms. 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
   Suvoda’s platform includes a comprehensive API-surface, using the latest cloud technologies.
   
   
2. The Virtual Partition: our unique 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. Suvoda’s proprietary low-code/no-code tools: making set-up customizations and mid-study changes simpler
   The tools allow our teams to:

• • • 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