ABOUT SUVODA
Suvoda is a global clinical trial technology company whose real-time experience platform empowers sponsors and CROs to make confident decisions and sites and patients to take calm, controlled action. Suvoda delivers interconnected, action-driven software solutions and industry-leading services and support, so that even in the most time-sensitive, mission-critical moments, life-changing studies keep moving forward. Headquartered outside Philadelphia, Suvoda also maintains offices in Portland, OR, Barcelona, Spain, Bucharest and Iasi, Romania, and Tokyo, Japan. The company maintains customer satisfaction scores that consistently exceed the technology industry average, contributing to the company being selected by trial sponsors and CROs to support 6000 trials across more than 115 countries. Suvoda recently merged with Greenphire, a leading provider of clinical trial financial management and patient support tools. To learn more, visit suvoda.com. Follow Suvoda on LinkedIn.
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Suvoda Announces Agentic RTSM, Enabling The Reduction Of Clinical Trial Startup Timelines By Up To 80%
The next evolution of Suvoda IRT is designed to accelerate study builds and change orders, elevate user experience, and deliver intelligent insights
FEATURED ARTICLES
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Late or missing reimbursements push patients out of trials. Real-time, flexible payments help keep them engaged and reduce site workload.
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For teams evaluating how to accelerate study startup without sacrificing rigor, this is a clear look at what AI-native trial technology makes possible now.
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Adaptive basket trials need real-time data to close underperforming cohorts fast. See how automation closes that gap and protects patients.
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Outdated budget data slows trial startup. Real-time market benchmarking helps sites and sponsors negotiate faster and get treatments to patients sooner.
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Manual outcome tracking creates compliance gaps and data quality risks. Electronic assessments help trial teams capture cleaner data, faster.
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Learn how protocol-driven IRT systems support supply management and randomization to help trial teams cut risk and costs.
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How Agentic RTSM cuts study build timelines by up to 80%, accelerating kickoff-to-UAT while maintaining compliance, quality, and auditability in clinical trials.
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Are you managing site payments with spreadsheets and manual processes? Discover how automation can reduce administrative burden, improve site relationships, and accelerate clinical trial operations.
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Discover how AI-native technology is accelerating study startup, streamlining operations, and helping sponsors and CROs deliver therapies to patients faster.
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Mastering the nuances between IRT and RTSM allows trial teams to move past confusing jargon and focus on the supply intelligence and randomization logic essential for study integrity.
CONTACT INFORMATION
Suvoda
181 Washington St., Suite 100
Conshohocken, PA 19428
UNITED STATES
NEWS
- Suvoda Patient App Earns "Best Patient Relationship Management Solution" In 2026 MedTech Breakthrough Awards Program
- Suvoda Announces Agentic RTSM, Enabling The Reduction Of Clinical Trial Startup Timelines By Up To 80%
- Suvoda Advances Clinical Trial Financial Planning With Support For Complex Multi-Payee Budgets
- Suvoda Named "Most Innovative Clinical Trial Technology Firm Of 2026"
- Suvoda Sets New Standard For Streamlined Patient And Site Experience In Clinical Trials
- Suvoda IRT Named A Leader In Everest Group's RTSM PEAK Matrix®
OUR PRODUCTS
ADDITIONAL PRODUCT INFORMATION
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A single mobile app simplifies clinical trial participation by unifying eConsent, IRT, and eCOA workflows, reducing patient burden and improving engagement across trial phases and locations.
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esigned for sponsors, CROs, sites, and patients, this modern solution delivers real-time data that supports crucial decisions during investigator grant budgeting, randomization, patient payments, and endpoint collection.
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Streamline trial budgets and payments with real-time fair market data, speeding startups and ensuring timely, transparent site funding worldwide.
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With the right IRT platform, you can handle inherent complexities and constant change, enabling confident decisions to move life-changing studies forward.