OUR PRODUCTS

IRT

Our advanced patient randomization and trial supply management system. Your clinical trial command and control center.
Trials conducted
1500+

in 87 countries

Average UAT defects
0.7

targeting ≤5 for moderate
& cosmetic defects

0n time delivery
100%

 for customer acceptance

EMPOWERING PRECISION

A centralized control center for patient and drug logistics, designed to harness the complexities of clinical trials and help advance human health.

Managing clinical trial randomization and supply logistics can be challenging, especially with the complexities of modern clinical trials. Hybrid trial approaches, tight timelines, and the need for mid-study adjustments mean that sponsors and sites need precise and powerful systems to keep trials running efficiently and on-time. 

From initial setup to mid-study adjustments to study completion, Suvoda Interactive Response Technology (IRT) gets the right drug to the right patient at the right time, with advanced randomization and drug supply management capabilities that integrate seamlessly with existing clinical workflows and eClinical systems. Suvoda IRT keeps trials running smoothly and supports sites, sponsors and CROs to:

  • Manage all clinical trial workflows efficiently, ensuring data is shared across systems
  • Meet exact trial randomization and drug supply needs with extensive configurability and customizability
  • More simply conduct patient visits and drug dispensation with an intuitive interface and user-centric design  
  • Access robust, real-time reporting for enhanced trial oversight and decision-making 

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ADVANCED ARCHITECTURE

Clinical trial complexity, meet our rich IRT functionality. Now you can address unique and changing needs—and hit tight timelines. 

A robust foundation of essential core IRT features, each focused on meeting the requirements of common protocols in decentralized, patient-centric trials. The tools to create new, client-custom functionality to support clinical research of increasingly novel, life-changing therapeutics. All developed as modular, easy-to-assemble building blocks. So our services teams can quickly launch systems that embrace the highest levels of protocol, operational, logistical, technical, and cultural complexity.  

What’s more, the Suvoda IRT system also includes extensive configurability options. It’s how we enable study teams to adjust system functionality over the lifespan of a trial to meet ever-changing demands. Because we know that no two of our clients’ trials start out exactly alike. We also know trials need to evolve, with mid-project course corrections to respond to the specific hurdles they encounter or insights they collect. And they all need to do so with speed and ease. 

 
Rich Functionality

Trial Logistics

  • Roles, permissions, and blinding management

  • Study and site administration

  • Cohort/stage/phase management

  • Dynamic cohort and dose management

  • Additional and dynamic visit schedule

Patient Logistics

  • Subject management

  • Adaptive replacement and randomization

  • Cross-over and re-treatment

  • Open-label extension

  • Dose calculation

  • Subject roll-over

  • Dose modification and interruption

Drug Logistics

  • 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

FLEXIBLE DESIGN

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.

ELEGANT INTERFACE

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.

irt-subjects-screenshot-1

 

INTELLIGENT REPORTING

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.

irt-reports-screenshot-1

 


FEATURED IRT MODULES
Temperature excursion management for IRT
Temperature Excursion Management

Take command of the cold supply chain

Easy IRT integration with temperature data loggers, temperature monitoring software, and depot distribution solutions
Temperature Excursion Management

Take command of the cold supply chain

Easy IRT integration with temperature data loggers, temperature monitoring software, and depot distribution solutions
Direct-to-patient shipping
Direct-to-Patient Shipping

Gain control in a world of decentralized trials

Intuitive tools to supply patients anywhere—at home or in the clinic—while protecting privacy and blinding
Direct-to-Patient Shipping

Gain control in a world of decentralized trials

Intuitive tools to supply patients anywhere—at home or in the clinic—while protecting privacy and blinding
At the very first presentation when we saw the system, is it strange to say that it seemed very beautiful? And very easy to use. The flow makes a lot of sense. Users can figure it out. The reports in particular are great, and I can control what I want to see.”
Niv Alon, Head of PMO, Galmed Pharmaceuticals
Related Insights

IRT: The key to wisely-managed patient interactions

Related Insights

IRT Buyer’s Guide

Make the best IRT decision to fit your clinical trial
A Single Clinical Trial Technology Platform

Powering the patient's digital journey in life-changing clinical trials.

Our eConsent, IRT, eCOA, and ePatient products are part of one dynamic clinical trial technology platform.
Client Services

Broad perspective. Keen insight. Calm guidance.

Client Services

Broad perspective. Keen insight. Calm guidance.

Integration

Seamless technology in complex ecosystems

Integration

Seamless technology in complex ecosystems

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