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.

Outcome:

• 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.