Systems Integration

Simplifying integrations within your evolving eClinical ecosystem

The complexity inherent in clinical trials for novel therapeutics isn’t just the result of their unique protocols. It also stems from the increasing numbers of technology systems that are critical to efficient operations and logistics in support of a more streamlined patient journey.

Implementations of the Suvoda Platform—and the suite of Suvoda IRT, eConsent, eCOA, and ePatient software we deliver through it— average two or more integrations per trial and up to ten for a single trial. Our experience spans EDC, depot, CTMS, lab vendors, and many other commercial and bespoke clinical trial systems. These reach across the full spectrum of study activities, from patient engagement, to supply management, to trial oversight.

Users experience integrations seamlessly within their Suvoda environment. Because ensuring that the right user—whether sponsor team member, site professional, or patient participant—is thoughtfully engaged, at the right moment, with the information and insights they need to calmly take the right next step, is just one more way we help everyone Trial wisely. 

Supported integrations:

Data management that supports your unique clinical trial protocols

Our Integration Team experts work hand-in-hand with a Suvoda Project Team dedicated to your trial to build integrations in parallel with study configuration. Together, we ensure both standardized and non-standardized integrations align with the specific functionality needed to ensure data flows between your eClinical ecosystem and Suvoda eConsent, IRT, eCOA, and ePatient software in a secure and compliant manner. 

The Suvoda Platform leverages standards-based REST API capabilities, enabling study teams and partner vendors to seamlessly integrate. Our multi-layered API security model supports robust data protection, with API authentication, permission-based authorization, and an API gateway that provides centralized access to eClinical data across the Suvoda Platform.

Our integrations, just like our software, are standardized for efficient reuse, while allowing configuration to meet the needs of a particular trial. Data transfers can be customized to occur at regular intervals—from minutes to months—and the data points, file format, and method can also be tailored for the greatest usability across your eClinical ecosystem. Two-way integrations are common, such as tracking shipment status data in our IRT system using courier info and tracking numbers, or using lab values from lab vendors, EDC, or CTMS software to adjust dosage or stratify subjects for randomization.