OUR PRODUCTS

RTSM (IRT) that takes weeks off study startup

Accelerate your study from contract to go-live–with agentic AI built for the most complex randomization and trial supply management.

 

Suvoda RTSM (IRT) supports sponsors and CROs

Start up studies faster

Handle any protocol, quickly

Give sponsors and sites their time back

Stay confident in the data

AI agents that cut kickoff-to-UAT timelines by up to 80%—so the path to first-patient-in is shorter.

Purpose-built for the most complex trials—oncology, CNS, rare disease—with the speed and flexibility to adapt when requirements change.

Sofia AI assistant. Faster access to trial information. Less administrative work. More room for the judgment calls that matter.

Real-time visibility across subjects, sites, drugs, and depots—so every decision is grounded in what's actually happening in your study.

AGENTIC AI FOR RTSM

The leading RTSM (IRT) that handles even the most complex protocols.

Clinical trials have never been simple. But getting a study off the ground—from contract to a working system—has always taken longer than it should. Configuration, manual testing, change orders, back-and-forth—all pull time away from what matters most: time with patients.

Suvoda RTSM changes that. It uses agentic AI to do the heavy lifting in study setup—so your team can focus on the trial, faster. Studies that once took months to set up can now be ready for User Acceptance Testing in as little as two weeks.

At its core, it does what Suvoda IRT has always done: gets the right drug to the right patient at the right time, across even the most complex protocols in oncology, CNS, and rare disease. Regardless of whether that’s complexity of the therapeutic area, operations, geography, or languages. What's new is the speed.

Suvoda RTSM—also referred to as IRT, or (Interactive Response Technology)—gives sponsors and study teams:

  • Faster study startup—agentic AI that cuts kickoff-to-UAT by up to 80%
  • A better experience for sponsors and sites—quicker access to information, with less friction throughout the study
  • Intelligent insights—real-time visibility into trial status and the decision-support to act on it
  • Complete IRT/RTSM functionality—built for complexity, adaptable when protocols change, and ready for the hardest trials

 

Throughout it all, Sofia, Suvoda's AI assistant, is embedded in the system. Ask it a question, pull a report, check depot inventory, or get a drug lot release in seconds. What used to take multiple screens and minutes of clicking is now a conversation.

AGENTIC AI ARCHITECTURE

Built for complexity. Accelerated by AI.

In Suvoda RTSM, multiple AI agents work in parallel to handle distinct phases of the study build—software configuration, customization, testing—and to turn around change orders mid-study. Because it's built on Suvoda's patented platform, it draws on what we've learned delivering thousands of trials. It doesn't start from scratch for each build. It starts from experience.

The result is a modular architecture that lets our services teams launch fast and adapt faster. When a protocol changes—and it will—mid-study amendments are a controlled, speedy process, not a project themselves.

 
Rich Functionality

Trial logistics

  • Agentic AI study build and configuration

  • Roles, permissions, and blinding management

  • Study and site administration

  • Cohort/stage/phase management

  • Dynamic cohort and dose management

  • Additional and dynamic visit schedule

  • Embedded, intuitive Sofia AI assistant 

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

  • Fast access to drug supply data and visualizations with Sofia AI assistant 

  • Drug supply forecasting

FLEXIBLE DESIGN

Built to embrace the unknown. Because your RTSM should be as ready for change as you are.

The scientific process isn't static. And neither is your trial. Protocols get amended. Doses change. Sites are added. That's why Suvoda RTSM is designed to adapt mid-study.

Permissioned users can make commonly-needed modifications and corrections directly in the system after go-live. No change order, no waiting. And when more significant updates are required, agentic AI can handle the configuration work, so what once stretched across weeks can now be done in a fraction of the time.

ELEGANT INTERFACE

Simple enough to use on day one. Powerful enough for your most complex protocols.

A well-designed RTSM/IRT system gets out of the way. It lets site coordinators, study teams, and even home caregivers focus on patients rather thanon navigating the software.

Suvoda RTSM is built with that in mind. Minimalist design, intuitive navigation, patient-centric workflows. Whether someone uses it every day or once a month, the experience is consistent and clear.

Sofia makes it faster still. Ask a question, pull trial data, compare depot inventories, review drug lot releases, create a graph—all in a conversation, without leaving the screen you're on. The study blind is protected. The answers are accurate. And what used to take several clicks now takes seconds.

Screenshot of IRT for clinical trials

 

INTELLIGENT REPORTING

Always know where you stand—and what to do about it.

Pre-set and ad-hoc reports in Suvoda RTSM give you real-time views of the data points, KPIs, and trends that matter most: subjects, sites, drugs, depots. What you need to manage today's trial—and plan tomorrow's.

With Sofia, those insights are even more accessible. Ask for a depot inventory summary, flag a supply risk, or pull a cross-site compliance view—in the interface, in seconds, without building a report from scratch.

Screenshot of IRT for clinical trials


FEATURED IRT MODULES
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

Everest Group RTSM PEAK Matrix®

Suvoda IRT has been named a Leader
Related Insights

IRT Buyer’s Guide

Make the best IRT/RTSM decision to fit your clinical trial.

RTSM FAQs

A UNIFIED CLINICAL TRIAL PLATFORM

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

Embrace today’s clinical trial complexities with a market-leading, real-time software platform to drive confident decisions and calm action.
Temperature excursion management for IRT
Temperature Excursion Management

Take command of the cold supply chain

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

Take command of the cold supply chain

Easy RTSM/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.
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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