COVID disruption and digitization acceleration made sponsors, sites and patients embrace technology like never before. Regulatory authorities’ attitude/approach and their comfort levels on “Data collection location - site vs home” changed as well. All these are positive signs for Clinical Research.
mIRT platform helps speeding up deployment of studies. Users can reduce the risks, burdens, complexities, work-load, time and costs linked with managing all facets of global patient randomization and clinical trial supply management.
The mIRT Advantage
mIRT Platform offers the industry’s best end-to-end, configurable IRT/RTSM solutions that covers the end-to-end life-cycle of supplies management from planning and supplies forecasting to inventory management as per the study protocol requirements, drug accountability, drug reconciliation and ensuring all regulatory requirements
mIRT Platform offers robust reporting with in-built and custom reporting. When it comesto integration, several industry stand EDC and CTMS systems have been already integrated. Seamless integration is important form IRT and sponsors alike as that will allow data consistency across your systems.
mIRT can be deployed in less than 2 weeks as some of the modules are “No Built” (also known as no code / low code). This accelerates timelines for sponsors and improves efficiency for CROs.
Take advantage of our competitive and fixed/unit pricing models to reduce the overall cost of IRT/RTSM ownership. With some of our versions there will be no change orders raise as this leads to predictable cost till study close out.
Innovation Meets Supplies Management
Reduce Drug Supply Overages, Outages by 30%
Reduce cost of ownership up to 40%
Bundle several studies and realize savings up to 50%
What We Offer
Our No-Build system is an upshot of vast amount of research put into clinical studies core functional areas, processes and pain points. Over the years, mIRT XPRESS has been designed, developed and evolved to be a robust product which is not just limited to a particular module but goes beyond and works as a one-stop solution for varied clinical study needs. Like a stimulator for improved study efficiencies and flexibility, it is a solution where one can configure the way they wants without depending on the developer or the vendor - as all setup is performed using UI.
mIRT is customized to provide the exact level of functionality required for your study to support unique, protocol-specific requirements of today’s complex clinical trial designs including advanced trial randomization methods(including custom algorithms), master protocols, basket trials, drug supplies management and simplify site, study, and subject management with real time tracking thereby allowing users perform day-to-day tasks more efficiently and cost effectively.
mIRT RAND provides a regulatory compliant cloud-based randomization software for clinical trials allowing you to configure your patient randomization lists as well as medication kit lists. Full support for open and double-blinded trials, customizable role-based access control, email notifications and real-time reporting functions are built-in.A simple and cost-effective alternative that can be used independently and comes with unlimited trial duration, number of subjects, clinical sites, treatment arms and stratification variables, all for a one-time fee.
mIRT Supplies is a purpose-built supplies forecasting and management tool with easy integration with other tools and lets you easily create and compare supplies scenarios against trial objectives much faster with multiple forecasting models considering various supply parameters to simulate multiple supply scenarios/requirements. This enables you to devise supply strategy that reduce drug waste and study costs considerably.Get user interactive view of your forecasts (Modified Holt, Moving Average, Inhibited, Croston, Others) complete with charts and graphs for better visibility across entire supply chain.
Let us show you how mIRT can help your study and corporate objective