RTSM

The Randomization and Trial Supply Management (RTSM) Clinical Trial Software streamlines the setup of randomization and supply management in clinical trials without the need for coding. This powerful and configurable solution helps in adapting to mid-study changes efficiently.

Seamless Participant Management

The system confirms participant eligibility, maintains balanced cohorts, and distributes dosing schedules efficiently.

Robust Randomization

Experience a range of randomization types to support complex studies and eliminate selection bias.

Supply Chain Optimization

Coordinate dispensing plans aligned with manufacturing, packaging, labeling, and logistics to meet the dynamic demands of clinical trials.

Minimize risk and maintain control over clinical trial supply management with no-code solutions providing precise automated randomization and inventory control. Ensure seamless investigational product delivery with proactive risk mitigation strategies.

Interactive Response Technology (IRT) for Any Study

This software optimizes supply management with automation, minimizes waste, aligns with site storage needs, and provides full oversight to eliminate bias and streamline reconciliation.

Enjoy real-time inventory tracking at all stages, ensuring products are in the right place, at the right time, paired with the appropriate temperature controls. The system integrates seamlessly with a Clinical Data Management System (CDMS) and Electronic Data Capture (EDC) for comprehensive trial oversight and data synchronization.

Medrio RTSM offers various features aimed at maintaining high standards of compliance and operational excellence while enhancing data quality, engagement, and retention.

• Automated expiry date management and shipment notifications.
• Site inventory resupply order automation.
• Temperature control with enforced log uploads and excursion alerts.

Testimonials highlight the ease of implementation, reliable timelines, and versatile data management, making it an attractive choice for efficient clinical trials.