About Our IWRS System

Our Interactive Web Response System (IWRS) is designed to streamline and control clinical trial operations through intelligent randomization, real-time inventory management, and automated workflow management.

500+
Daily Randomizations
Multi-arm
Study Designs
Real-time
Supply Control
ICH-GCP
Compliant

Key Features

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Real-time Randomization
Instant, protocol-driven subject randomization at the site level.
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Role-Based Access Control
Secure access for sites, monitors, sponsors, and supply managers.
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Built-in Audit Trail
Full traceability of randomization and supply transactions.
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Automated Visit & Dosing Control
Protocol-compliant visit scheduling and dosing enforcement.
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Flexible Study Configuration
Configurable study designs, cohorts, and treatment arms.
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Real-Time Reporting & Alerts
Instant notifications for enrollment, drug supply, and milestones.

System Architecture

Designed for high availability, regulatory compliance, and global trial operations.

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Modular Microservices
Scalable architecture supporting complex trial workflows.
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Hybrid Data Storage
Optimized storage for subject, treatment, and supply data.
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Secure Cloud Hosting
Global access with enterprise-grade security and uptime.

Benefits for Sponsors & CROs

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Faster Study Start-up
Rapid study setup and protocol configuration.
visibility
Real-time Monitoring
Complete visibility into enrollment and treatment assignment.
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Improved Data Quality
Eliminates randomization and dosing errors.
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Cost Savings
Reduced operational overhead and drug wastage.
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Regulatory Compliance
Fully compliant with ICH-GCP and 21 CFR Part 11.
IWRS Platform

Automate your trial randomization today.

Our IWRS ensures error-free, protocol-compliant randomization and supply management for clinical trials of any scale.

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