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RTSM/IRT
Clinical Supply software

Last few years rapid digitization has led sponsors, sites, and patients to embrace technology more than ever. Regulatory authorities have also adapted to changing data collection methods, whether at the site or home. These shifts signal positive advancements in clinical research.

mIRT (RTSM software) accelerates deployment of clinical studies while reducing risks, burdens, complexities, workload, time, and costs associated with global clinical trial supply management and patient randomization.

mIRT
Advantage

End-To-End Solution with a Modular Approach

mIRT offers an industry-leading, end-to-end interactive response technology in clinical trials, covering the full lifecycle of clinical supplies software management. From planning and forecasting to inventory management, drug accountability, and regulatory compliance, mIRT ensures seamless RTSM clinical trials operations.

Integration & Reporting

mIRT provides robust, in-built, and customizable reporting features. It seamlessly integrates with industry-standard EDC and CTMS systems, ensuring data consistency and smooth operations between RTSM software and sponsor systems.

Rapid Start-Up

With its no-code/low-code modules, mIRT can be deployed in under two weeks. This rapid implementation benefits sponsors and improves operational efficiency for Clinical managers.

Reduced Cost of Ownership

Our competitive, fixed, and unit-based pricing models help lower the overall cost of RTSM clinical trials. With certain versions, there are no change order costs, ensuring predictable expenses until study closeout.

Innovation Meets Clinical Supplies Management

Reduce-Drug-Supply-Overages

Reduce drug supply
overages and outages by
30%

Reduce-cost-of-ownership

Lower cost of
ownership by up to
40%

Bundle-several-studies

Bundle multiple studies and
achieve savings of up to
50%

What We Offer

mIRT-Xpress-logo-min

Our No-Build system is designed from extensive research into clinical trial supply management pain points. mIRT Xpress provides a robust, ready-to-use platform that eliminates dependency on developers or vendors. Users can configure it as needed using an intuitive UI, enhancing study efficiency and flexibility.

mIRT is tailored to meet protocol-specific requirements, supporting advanced randomization methods, master protocols, basket trials, and complex drug supply management. With real-time tracking, site, study, and subject management become more efficient and cost-effective.

mIRT-Custom-logo-min
mIRT-Supplies-min

mIRT Supplies is a specialized clinical supplies software for forecasting and managing supplies. It integrates with other tools and allows users to create and compare supply scenarios against trial objectives. Multiple forecasting models, including Modified Holt, Moving Average, and Croston, provide an interactive, visual approach to optimizing supply chain strategies and reducing waste.

Experience how mIRT enhances clinical trial supply management with efficiency and cost-effectiveness.

Contact Us

Frequently Asked Questions

faq-question

What is DDi’s mIRT (RTSM/IRT Clinical Supply software)?

DDi’s mIRT is an industry-leading Interactive Response Technology (RTSM/IRT) software designed to accelerate clinical study deployment while reducing risks, complexities, and costs associated with global patient randomization and clinical trial supply management.
faq-question

How does mIRT help reduce drug supply overages and outages?

mIRT utilizes advanced forecasting models (such as Modified Holt, Moving Average, and Croston) to help clinical teams create and compare supply scenarios against trial objectives, reducing drug supply overages and outages by up to 30% through real-time tracking and optimization.
faq-question

What are the deployment benefits of the mIRT Xpress “No-Build” system?

The mIRT Xpress platform provides a ready-to-use system designed from extensive clinical supply research. It eliminates dependency on custom developers or vendors, allowing users to configure studies flexibly using an intuitive UI for rapid start-up.
faq-question

What trial designs and randomization methods does mIRT support?

mIRT is tailored to protocol-specific requirements, supporting advanced randomization methods, complex drug supply chains, master protocols, basket trials, and comprehensive site, study, and subject management.
faq-question

What financial and operational savings can sponsors achieve using mIRT?

Sponsors can lower total cost of ownership by up to 40%, reduce drug supply waste and overages by 30%, and achieve savings of up to 50% by bundling multiple clinical studies onto the platform.

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