Interactive Web Response System (IWRS)

Streamlined Clinical Trial Management Platform. At Sourcetranscript, we specialize in delivering advanced, secure, and compliant digital solutions for the clinical research industry.

Empowering Clinical Trials with Technology

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About Sourcetranscript

At Sourcetranscript, we specialize in delivering advanced, secure, and compliant digital solutions for the clinical research industry. Our flagship product, the Interactive Web Response System (IWRS), is designed to support sponsors, CROs, and investigative sites in streamlining clinical trial operations from start to finish.

Our IWRS System at a Glance

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Patient Management

Real-time tracking of subject enrollment, visits, and treatment assignments.

Randomization Engine

Supports various methods including block, stratified, and dynamic randomization.

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Drug Supply Management

End-to-end visibility and control over investigational product distribution and resupply.

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Compliance & Security

Built to meet 21 CFR Part 11, ICH-GCP, and GDPR standards.

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User-Centric Experience

Intuitive UI, responsive design, and role-based access to ensure simplicity and security for every user.

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Scalable Architecture

Powered by .NET, Clean Architecture, and Microsoft SQL Server to handle complex and global trial demands.

Benefits of Using IWRS

Improved data accuracy

Enhanced validation and real-time checks ensure the highest quality data capture.

Reduced operational burden

Automated workflows and intuitive interfaces reduce manual efforts and errors.

Faster site activation and enrollment

Streamlined processes accelerate study startup and subject recruitment.

Enhanced subject safety

Real-time monitoring and alert systems protect participant welfare.

Scalability for global trials

Cloud-based architecture supports multi-site, multi-country studies.

Key Features

✨ Transforming Clinical Research Through Innovation

  • Automated Data Validation
  • User friendly UI/UX
  • Patient Management
  • Drug Supply & Inventory Management
  • Customizable Data Fields
  • Documentation and Reporting
  • Data Export
  • Compatibility with Legacy Systems
  • Audit Trail & Compliance (21 CFR Part 11, GCP, GDPR)
  • Role-Based Access Control
  • Emergency Unblinding Workflow
  • Multisite & Multilingual Support
  • Real Time Reporting & Alerts(Email)