Trial wisely

When the only constant is complexity, Suvoda’s platform-based IRT, eConsent, eCOA, and ePatient solutions helps clinical trial sponsors, sites, and patients gain calm, confident control
PLATFORM + PRODUCTS + PROCESS + PEOPLE

An elegantly-architected platform. Precision-built products. Rigorously-defined processes. And exceptionally-prepared people. It’s how, at Suvoda, we empower sponsors, sites, and patients to more artfully take command over infinite, interdependent, and ever-changing variables. Across the full lifespan of your study, you’ll find every minute of every day is calmer and more controlled.

PLATFORM + PRODUCTS + PROCESS + PEOPLE

An elegantly-architected platform. Precision-built products. Rigorously-defined processes. And exceptionally-prepared people. It’s how, at Suvoda, we empower sponsors, sites, and patients to more artfully take command over infinite, interdependent, and ever-changing variables. Across the full lifespan of your study, you’ll find every minute of every day is calmer and more controlled.

An Urgent Focus

The mission-critical, time-sensitive, and deeply-human interactions that move life-changing studies forward

At Suvoda, we find that the most difficult things are often the most important—and rewarding—things to do.

We founded our business by taking on randomization and drug supply complexities in oncology, CNS, and rare disease studies. We delivered one of the industry’s premiere IRT solutions—a unique combination of software, standards, and support. With Suvoda IRT, sponsor teams and site professionals found it easy to get and give the right drug dose right where and when a patient is ready for a treatment.  

As we’ve expanded our portfolio, we’ve continued to apply our proven Suvoda approach to similar mission-critical, time-sensitive, and deeply-human moments in clinical trials—the urgent moments, like informed consent, visit scheduling, outcomes reporting, and patient payment, that if missed, can both stall science and upend lives.  

Today, the Suvoda Platform and our IRT, eConsent, eCOA, and ePatient product suite embraces the inherent complexity in life-changing trials, harnessing it to transform the journey for everyone involved. The result? Sponsor teams, site professionals, and patient participants alike can make more informed, more nuanced decisions. They can smoothly and seamlessly take urgent action, no matter where they are, right when it’s required. In short, they can Trial wisely—and ultimately, better help advance human health.

CLIENT SERVICES

A team that stays with you for the lifespan of your trial

Bringing broad perspective, keen insight, and calm guidance to your team, your sites, and their patients.
CLIENT SERVICES

A team that stays with you for the lifespan of your trial

Bringing broad perspective, keen insight, and calm guidance to your team, your sites, and their patients.
Standards & Metrics

Delivering to the highest of clinical trial quality levels

Clear operating guardrails free our team members, customers, and partners to achieve greater success.
Standards & Metrics

Delivering to the highest of clinical trial quality levels

Clear operating guardrails free our team members, customers, and partners to achieve greater success.
There’s some kind of process with their training that really works. They’re so proactive, asking us ‘What about this or that?’ … They’re a bonafide partner.”
RICK O’HARA, DIRECTOR, R&D BUSINESS OPERATIONS, ENDO

  

Partner Network

Speeding implementation—and innovation—in trials

Partner Network

Speeding implementation—and innovation—in trials

Integration

Seamless technology in complex trial ecosystems

Integration

Seamless technology in complex trial ecosystems