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IRT for Clinical TrialsY-Prime

YPrime IRT is a cloud-based interactive response technology solution designed to manage subject randomization and clinical trial supply logistics. It supports allocation of participants to treatment arms, drug inventory tracking, and distribution workflows across study sites. The system operates within regulated clinical research environments and integrates with other clinical trial technologies to provide centralized operational control.

Vendor

Vendor

Y-Prime

Company Website

Company Website

Product details

YPrime IRT is a cloud-based interactive response technology solution designed to manage subject randomization and clinical trial supply logistics. It supports allocation of participants to treatment arms, drug inventory tracking, and distribution workflows across study sites. The system operates within regulated clinical research environments and integrates with other clinical trial technologies to provide centralized operational control.

Key Features

Subject Randomization Automates participant assignment to study arms.

  • Configurable randomization schemes
  • Stratification support
  • Blinding management

Clinical Supply Management Controls investigational product inventory and distribution.

  • Drug shipment tracking
  • Depot and site inventory oversight
  • Expiry date monitoring

Study Design Configuration Supports complex protocol requirements.

  • Adaptive trial design support
  • Cohort management
  • Visit scheduling logic

Real-Time Inventory Visibility Provides operational transparency.

  • Dashboard reporting
  • Stock level alerts
  • Resupply triggers

Role-Based Access Control Ensures appropriate system permissions.

  • Site-level access
  • Sponsor and CRO oversight
  • Audit trail tracking

Integration Capabilities Works within broader clinical ecosystems.

  • Integration with eCOA and eConsent
  • Data exchange with EDC systems
  • API-based connectivity

Regulatory & Compliance Controls Designed for regulated environments.

  • 21 CFR Part 11 support
  • Secure electronic records
  • Full audit logs

Benefits

Improved Allocation Accuracy Reduces manual errors in treatment assignment.

  • Automated logic execution
  • Controlled blinding processes

Optimized Drug Supply Management Minimizes waste and shortages.

  • Real-time inventory tracking
  • Automated resupply workflows

Operational Efficiency Centralizes study supply oversight.

  • Reduced manual coordination
  • Faster study execution

Enhanced Study Control Supports complex and adaptive trial designs.

  • Flexible configuration
  • Immediate access to study metrics

Regulatory Readiness Maintains compliant documentation and tracking.

  • Secure audit trails
  • Controlled user permissions

Scalable for Global Trials Supports multinational site networks.

  • Multi-site configuration
  • Global inventory management