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Modernization of Enterprise Collaboration Platform for Pharmaceutical Data Management
  1. case
  2. Modernization of Enterprise Collaboration Platform for Pharmaceutical Data Management

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Modernization of Enterprise Collaboration Platform for Pharmaceutical Data Management

nix-united.com
Medical
Information technology

Legacy System Limitations and Data Fragmentation

Thomson Reuters' JPharm platform suffered from a lack of technical documentation, heterogeneous data sources causing manual data processing delays, and an outdated architecture that hindered scalability and maintenance. Previous vendor attempts at modernization failed due to coordination issues and insufficient technical expertise.

About the Client

Global provider of pharmaceutical market tracking and collaboration solutions with operations in research, regulatory compliance, and drug development support

Platform Modernization Goals

  • Reverse-engineer legacy system architecture for documentation
  • Integrate fragmented data sources into a cohesive system
  • Implement scalable architecture for future expansion
  • Automate data loading processes for editorial teams
  • Establish technical roadmap for continuous development

Core System Requirements

  • Reverse-engineered system architecture documentation
  • Centralized data management interface
  • Automated data validation and formatting modules
  • Scalable microservices-based architecture
  • Role-based access control for global editors

Technology Stack

Java
PL/SQL
Microservices Architecture

System Integrations

  • Legacy database migration tools
  • Cortellis collaboration ecosystem APIs
  • Global user authentication system

Quality Attributes

  • 99.9% system availability SLA
  • Support for 10x concurrent user growth
  • HIPAA-compliant data handling
  • Automated CI/CD pipeline implementation
  • Documentation-driven development standards

Business Transformation Outcomes

The modernized platform will enable real-time pharmaceutical data collaboration across global teams, reduce manual data processing time by 70%, and establish a foundation for AI-driven drug discovery integrations. The architecture overhaul will support 5-year scalability requirements while maintaining regulatory compliance and reducing technical debt by 60%.

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