MINERVATE
Minervate's IRT platform enables intelligent randomization, automated supply management, and real-time study control — designed for modern clinical trials with full regulatory compliance across global studies.
Request a DemoEverything you need to run efficient, compliant, global clinical trials.
Advanced algorithms supporting stratified, block, and adaptive trial designs.
Automated kit assignment, depot management, and predictive resupply logic.
Multi-region trial coordination, enrollment caps, and site activation.
Real-time enrollment and inventory dashboards with exportable reports.
Full audit trails, role-based permissions, and validation-ready architecture.
Seamless connectivity with EDC, ePRO, CTMS, and EHR platforms.
Explore the full scope of what Minervate IRT delivers.
Configure stratified, block, and adaptive randomization with automated subject allocation. Supports complex multi-arm, multi-stage designs with real-time audit logging.
Automated kit assignment, depot and site inventory tracking, and predictive resupply logic to prevent stockouts and reduce waste across all trial locations.
Control enrollment caps, manage site activation and deactivation, and coordinate regional supply distribution across multiple countries and time zones.
Live dashboards covering enrollment, randomization, and supply status. Exportable reports for sponsors, monitors, and regulatory submissions.
Role-based access control, full audit trails, electronic signatures, and a validation-ready architecture compliant with FDA 21 CFR Part 11, HIPAA, and GxP standards.
Let Minervate IRT handle the complexity so your team can focus on what matters — delivering results for patients.
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