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 — ensuring accuracy, compliance, and efficiency across every study phase.

Key Features

Real-time Randomization

Instant, protocol-driven subject randomization at the site level

Role-Based Access Control

Secure access for sites, monitors, sponsors, and supply managers

Built-in Audit Trail

Full traceability of randomization and supply transactions

Automated Visit & Dosing Control

Protocol-compliant visit scheduling and dosing enforcement

Flexible Study Configuration

Configurable study designs, cohorts, and treatment arms

Real-Time Reporting & Alerts

Instant notifications for enrollment, drug supply, and milestones

System Architecture

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

Modular Microservices

Scalable architecture supporting complex trial workflows

Hybrid Data Storage

Optimized storage for subject, treatment, and supply data

Secure Cloud Hosting

Global access with enterprise-grade security and uptime

Benefits for Sponsors & CROs

Faster Study Start-up

Rapid study setup and protocol configuration

Real-time Monitoring

Complete visibility into enrollment and treatment assignment

Improved Data Quality

Eliminates randomization and dosing errors

Cost Savings

Reduced operational overhead and drug wastage

Regulatory Compliance

Fully compliant with ICH-GCP and 21 CFR Part 11