in 80 countries
Average UAT defects
targeting ≤5 for moderate
& cosmetic defects
0n time delivery
for customer acceptance
Clinical trial complexity, meet our rich IRT functionality. Now you can address unique needs—and hit tight timelines.
A robust foundation of essential core IRT features. Each focused on meeting the requirements of common protocols in complex decentralized, patient-centric trials for therapeutic areas such as oncology, central nervous system, and rare disease. The tools to create new, client-custom functionality. All developed as easy-to-assemble building blocks. So our services teams can support the unique needs of each trial.
In addition to an advanced architecture that allows for fast and comprehensive functionality, our IRT system also includes extensive configurability options. It’s how we enable study teams to adjust system functionality to meet the ever-changing demands of their trial. Because no two of our clients’ trials are exactly alike, but all share a world of complexity. And all need to move with speed.
- Roles, permissions, and blinding management
- Study and site administration
- Cohort/stage/phase management
- Dynamic cohort and dose management
- Additional and dynamic visit schedule
- Subject management
- Adaptive replacement and randomization
- Cross-over and re-treatment
- Open-label extension
- Dose calculation
- Subject roll-over
- Dose modification and interruption
- Drug dispensing management
- Drug supply management
- Drug accountability, reconciliation, and returns/destruction management
- Temperature excursion management
- Controlled substance management
- Variable drug sourcing
- Central pharmacy
- Direct-to-patient shipping
- Robust supply strategy management
Built to embrace the unknown. Because your IRT should be as ready for change as you are.
The scientific process isn’t static. And neither is your trial. To collect the richest data, protocols must be amended as new information is obtained. That’s why we designed the Suvoda IRT to adapt mid-study with ease.
Commonly-needed additions, modifications, and corrections to study, site, drug management, and administrative functions can be made by permissioned users within our system after go-live. This puts control in your hands and reduces the time and costs associated with change-orders. And if more significant updates are required, our modular architecture makes it a simple and speedy process for your dedicated Suvoda project team to add in new IRT features.
A user-friendly IRT experience eases decisive action for users of all experience levels.
We find that people are more likely to work at their best when they’re using the tools they like best.
That’s why, no matter the level of experience with clinical trial technology—from dedicated pros to more occasional site-users, and even home caregivers—you’ll find interactions with the Suvoda IRT are universally simple. It’s the result of a minimalist look and feel, intuitive navigation, and patient-centric workflow. And it’s all intended to drive focus on the immediate task at hand.
See the way to long-term trial performance, in real time, with pre-set and ad-hoc reports and advanced analytics.
Suvoda IRT pre-set and ad-hoc reports give you up-to-the-minute visualizations of data points, KPIs, and trends on the subjects, sites, drugs, and depots within a given study. It’s how you’ll always know where you stand—and what needs your attention.
Why such robust reporting? To give you the intelligence you need to make better decisions in executing on today’s trials—and planning for tomorrow’s.