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Development of a Scalable Cloud-Based Content Management System for Pharmaceutical Advertisement Review and Compliance
  1. case
  2. Development of a Scalable Cloud-Based Content Management System for Pharmaceutical Advertisement Review and Compliance

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Development of a Scalable Cloud-Based Content Management System for Pharmaceutical Advertisement Review and Compliance

danavero
Medical
Information technology
HealthCare

Challenges in Pharmaceutical Advertisement Review Process

Need to manage complex workflows for pharmaceutical advertisement approval with stringent regulatory requirements, cross-team collaboration challenges, regional compliance variations, and structured claims tracking with evidence linking in a globalized market.

About the Client

Global provider of analytics, technology solutions, and clinical research services for the life sciences industry

Project Goals for Enhanced Content Management

  • Create a cloud-based CMS tailored for pharmaceutical advertisement review
  • Enable annotation capabilities for medical/legal reviewers
  • Implement evidence linking for advertisement claims
  • Ensure scalability for global enterprise clients
  • Support multi-regional regulatory compliance frameworks

Core System Functionalities

  • Interactive annotation tools for advertisement markup
  • Evidence-document linking with version control
  • Multi-stage approval workflow engine
  • Regulatory compliance checklist builder
  • Multi-language content management
  • Audit trail for claim-evidence relationships

Technology Stack Requirements

Cloud-native architecture
React
Java
Spring Framework
PostgreSQL
DevOps automation

System Integration Needs

  • Regulatory database APIs
  • Enterprise authentication systems (SSO)
  • Cloud storage services
  • Analytics platforms

Operational Requirements

  • High scalability for concurrent global users
  • Enterprise-grade security with HIPAA/GDPR compliance
  • 99.9% system availability SLA
  • Role-based access control (RBAC)
  • Multi-tenancy architecture support

Expected Business Impact of the New CMS

Streamlined pharmaceutical advertisement approval workflows with 40% reduced processing time, ensured compliance with global regulatory standards, enhanced cross-functional collaboration through centralized evidence management, and established scalable infrastructure supporting 1000+ concurrent enterprise users worldwide.

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