Suvoda Products
Suvoda eConsent
Suvoda eConsent is designed to improve patient comprehension and simplify consent management for sponsors and sites without the need to change existing processes.
Sponsors and sites can give patients the tools they need to understand complex study information through robust functionality including embedded videos, FAQs, in-document discussion threads, and a cross-linked glossary.
Unified with Suvoda IRT on the patented Suvoda Platform, Suvoda eConsent enables real-time visibility into and automated control over the patient consent and re-consent process—helping to reduce regulatory risk and administrative burden.
Suvoda IRT
Suvoda IRT is purpose-built to harness the complexities of today’s patient-centric trials, empowering sponsors, CROs, and sites to take full command of patient and drug logistics. And now with Sofia, Suvoda’s safe and secure AI assistant in the early adopter stage, drug supply managers can have efficient access to vital information through an intuitive chat interface.
Our approach is built upon an extensive, ever-expanding library of IRT features and a dedicated services team that supports the unique needs of each trial throughout its duration.
Suvoda IRT is built on the patented Suvoda Platform, a single clinical trial technology platform that delivers a seamless experience, streamlines integrations with a comprehensive API surface, and drives data integrity through a single, robust data model.
Suvoda eCOA
Purpose-built with users at the center, Suvoda eCOA makes it easier and more efficient to get quality patient outcomes data for submissions and approvals.
And when eCOA + IRT are unified on the patented Suvoda Platform with a shared data layer, outcomes data is seamlessly shared in real-time to inform critical trial decisions in IRT like screening, randomization, and dose modifications. The shared data layer also minimizes data entry errors and increases data accuracy and integrity.
Suvoda eCOA combines intuitive design and robust functionality with expert scientific & operational guidance and a dedicated licensing & localization team. And the patented Suvoda Questionnaire Design Language (SQDL) expedites questionnaire design and deployment.
Available through the Suvoda app on iOS and Android, Suvoda eCOA is designed for global deployments and supports BYOD, provisioned device, and hybrid models.
Greenphire Patient Payments
Greenphire Patient Payments combines an internationally accessible and easy-to use-portal, flexible payment methods—including the widely adopted ClinCard, and global expertise and consultative support to simplify payment operations and boost patient engagement.
A part of the unified Suvoda Platform, Greenphire Patient Payments enables you to pay participants in real time, reduce manual administrative tasks for site staff, and gain complete financial transparency and control.
Greenphire Travel
Greenphire Travel is a comprehensive service that delivers global travel and logistics support for patients and caregivers throughout a trial.
Our offering removes the burden of coordinating travel arrangements for sites and patients, while covering all expenses up front. From rideshare and trains to international flights and visa services, we offer a wide range of options and delivery models to make sure that each patient’s needs are met.
With dedicated local language support staff, travel partners, and concierge coordinators stationed around the world, we are committed to providing the best possible experience for every patient. As part of the unified Suvoda Platform, we aim to remove the logistical and administrative barriers that stand in the way of trial participation.
Suvoda Scheduling
Suvoda Scheduling equips study participants with one application to manage and schedule their clinical trial appointments from their own device.
Housed within the Suvoda Platform, its elegant design and powerful features, including configurable reminders and ability to sync multiple practitioner calendars also mean sites can spend less time administering their trials and more time with their patients.
Site Payments
As part of the Greenphire Clinical Finance Suite, our Site Payments solution brings simplicity, accuracy, and clarity to the traditionally manual, time-consuming process of executing investigator grants for research sites around the world.
By introducing globally compliant invoice and payment automation, you will be able to more easily scale your financial operations, turning site payments into a top-performing function of your business.
Our built-for-purpose technology has the sophistication to meet regional preferences and regulatory requirements, instilling confidence that your sites around the world will be paid on time, accurately, and with reduced administrative burden—driving site sustainability and overall trial efficiency.
Budgeting & Benchmarking
A core component of the Greenphire Clinical Finance Suite, our Budgeting & Benchmarking solution enables you to generate accurate budget estimates for your study based on the industry's most trusted fair market value (FMV) dataset.
Our Budgeting & Benchmarking product provides a powerful, data-driven foundation for your investigator grant budgets. Navigate from protocol to a defensible estimate with confidence and speed, empowering your team to gain stakeholder alignment, accelerate negotiation cycles, and reach the first patient in (FPI) milestone faster.