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One client in the pharmaceutical industry wanted a scalable and reliable system architecture, hassle free production and process compliance with US-FDA and EU systems.



  • Engineering and commissioning of Automation system with totally distributed architecture as per 21 CFR Part 11 guidelines.
  • Precise Batch Reports, Acute Raw Material Consumption Tracking, ClP Validation were implemented as per US-FDA Guidelines and GMP.
  • Centralized Data Logging of Process Values, Batch Trends, Supervisory control, User Administration was provided.
  • Intuitive interface required for almost zero training and provided single click diagnostics.