Suvoda LLC , a global clinical trial technology company specializing in complex studies in therapeutic areas such as oncology, central nervous system (CNS) and rare diseases, today launched a software platform specifically designed to provide clinical trial sites and sponsors with an easy way to manage complex, critical and time-sensitive moments in the patient journey.
Building on more than a decade of experience since the launch of its innovative IRT solution, and having supported more than 1,000 trials in 80 countries, Suvoda introduces a low-code/no-code platform to the eClinical market by unifying its eConsent, IRT solutions and eCOA. Designed to address the real challenges clinical trials face, the Suvoda Platform minimizes friction through the user experience, while reducing and simplifying integrations, and strengthening data governance, so studies they can be deployed more efficiently and with less risk of downtime.
“Clinical trials are becoming more complex, expensive, and fraught with challenges that affect trial execution: mid-study changes, data silos, trial delays, etc.” said Jagath Wanninayake, CEO of Suvoda. “To address these challenges, our team organically built a platform on which we are delivering the next generation of clinical trial applications designed to handle complexity with ease, and reduce overall risk across trials. Our goal is as long as patrons and users of the center spend less time with technology and more time on what’s most important to them…discovering scientific breakthroughs and focusing on the patients we all ultimately serve.”
The Suvoda Platform allows Suvoda’s IRT, eConsent and eCOA solutions to work seamlessly together and in harmony with other applications, to be easily adapted to the needs of each protocol and to be upgradeable to benefit from continuous improvements. The Suvoda platform offers a number of advantages, including:
Improved user experience and reduced workload. The new platform enables single sign-on and provides a consistent interface across all of Suvoda’s eConsent, IRT and eCOA solutions, with seamless user workflows that allow clinicians to seamlessly transition from one task to the next. This reduces workload and training so centers can spend more time on research and patients.
Rapid design and deployment of complex assays. The platform’s low-code/no-code technology streamlines study start-up and mid-study changes for even the most complex assays, while advanced design tools make customizations more convenient and standards one of the easiest sponsors to implement. A harmonized deployment process across all three solutions saves study teams time and effort.
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Improved data workflow and reduced integrations. Suvoda’s unified platform enables all patient and facility data from eConsent, IRT and eCOA to be centrally collected, managed, analyzed and stored. This is expected to result in better data governance for patrons, provide centers with access to real-time information, and offer a stronger eClinical ecosystem. In addition, clients benefit from three already integrated solutions: eConsent, IRT and eCOA, while the platform’s extensive API surface simplifies other necessary integrations with third-party solutions and sponsor systems.
eClinical programs prepared for the future. Platform users will always have the latest assay technology with Suvoda as updates can be made throughout the life of the assay without losing customizations. Additionally, with release opt-in, customers can choose which updates to accept, giving them control of their internal validation, acceptance, and training processes. Finally, Suvoda makes enterprise standards implementation future-proof by allowing sponsors to upgrade while maintaining their own processes and standards across all products built on the Suvoda platform.
“Whether it’s sponsors, CROs, site teams or patients, users expect a seamless trial experience digitally and in person, so we’ve designed the new platform to deliver just that,” said Andrew McVeigh , chief architect of Suvoda. “Suvoda offers a powerful test management platform that feels like a consumer app because we’ve put the user at the center of our design. Our robust back-end and intuitive design puts more control in the hands of our customers and offers the ability to manage trials of any level of complexity”.