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In an era of improved regulations to guarantee patient safety, clinical trials have become increasingly complex . As study sponsors now aim to meet multiple objectives, the level of complexity grows, clinical supplies strategy should be supported by automated systems to facilitate the process at the site and depots likewise offer more visibility across the supply chain, leading to better quality control. With Direct-to-patient as trend that will stay, systems need to have these built-in and not as special projects
As Custom as Your study!
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.
Unlike other IRT Tools, mIRT system allows sponsors get a high amount of visibility during development to customize or make adjustments as needed. mIRT delivers working study prototype faster than any custom built IRT - Set up, test, and deploy study protocols within weeks instead of months with innovative customization.
Adaptive & Complex Trials
mIRT supports adaptive and complex protocol designs with configurability, drug pooling strategies and program-based supply management. mIRT makes it easy to manage cohorts, add/delete new treatment arms or kit types, allocate or add drug supplies across multiple trials and more.
Direct to Patient
IRT for Direct-to-Patient module helps manage DtP services get investigational medicinal products (IMP) directly delivered to a patient’s home to counter pandemic situation and reduce risk associated in travelling directly to a site.
Advanced Technology
Cloud-based, easily configurable and advanced integration features enabling real-time access to study data and admin tools through mobile interface and to monitor your study’s advancement to make important decisions.
Features Include
All detailed functionality of Randomization, subject management, supplies management, reconciliation are included- Integration with several 3rd party EDC systems in market currently
- Automated and customizable supply/re-supply schemes
- Trial intelligence and Custom Reporting with Analytics
- Powered with eCOA and ePRO
- Can be integrated with data from wearable
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