It integrates randomization and trial supply management into a single, modular platform that is quick to configure and highly adaptable to the needs of different studies.

Key Features

• Randomization:
  • Flexible Randomization Methods: Supports various randomization methods, including stratified, block, and dynamic randomization, ensuring that studies can be tailored to specific requirements.
  • Real-Time Randomization: Provides real-time randomization capabilities, allowing for immediate assignment of subjects to treatment groups.
• Supply Management:
  • Inventory Tracking: Manages the entire lifecycle of clinical supplies, from initial shipment to site inventory and subject dispensing.
  • Automated Resupply: Automates resupply calculations and shipments, ensuring that sites always have the necessary supplies without overstocking.
  • Temperature Monitoring: Tracks and monitors the temperature of sensitive supplies, ensuring compliance with storage requirements.
• Modular and Configurable:
  • Quick Configuration: Allows for rapid setup and configuration, enabling teams to implement the capabilities they need in fast startup timelines.
  • Scalability: Scales to accommodate studies of all sizes and complexities, from small early-phase trials to large global studies.
• User-Friendly Interface:
  • Intuitive Design: Features an intuitive interface that simplifies the management of randomization and supply processes, reducing the learning curve for users.
  • Real-Time Dashboards: Provides real-time dashboards and reporting tools, offering visibility into study progress and supply status.
• Integration and Connectivity:
  • Seamless Integration: Integrates with other Veeva Vault applications, such as Vault EDC and Vault CTMS, ensuring a unified approach to clinical trial management.
  • Data Synchronization: Ensures that data is synchronized across systems, reducing manual data entry and the risk of errors.

Benefits

• Enhanced Efficiency: Streamlines randomization and supply management processes, reducing administrative burden and speeding up trial execution.
• Improved Compliance: Ensures compliance with regulatory requirements through automated tracking and monitoring of supplies.
• Better Decision-Making: Provides real-time insights into study progress and supply status, enabling proactive decision-making.
• Reduced Costs: Optimizes supply management, reducing waste and minimizing costs associated with overstocking or supply shortages.