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Pharmaceutical & Life Sciences Engineering

Pharmaceutical manufacturing demands strict sterile environmental compliance, automated electronic batch records (EBR), Water-for-Injection (WFI) loop regulation, and validated Clean-In-Place / Steam-In-Place (CIP/SIP) routines adhering to cGMP and FDA 21 CFR Part 11 standards.

Pharmaceutical & Life Sciences
Pharmaceutical & Life Sciences Architecture

Pharmaceutical & Life Sciences Engineering

On-Site Deployment in Turkey & Pakistan

Common Operational Challenges in Pharmaceutical & Life Sciences

•Rigorous cGMP & FDA 21 CFR Part 11 electronic signature audit compliance
•Sterile cleanroom differential air pressure cascades and humidity drift
•Critical Water for Injection (WFI) and purified water loop conductivity tracking
•High-speed tablet press and blister packaging synchronization downtime

Automation Solutions

  • 21 CFR Part 11 Validated SCADA & Electronic Batch Records (EBR)
  • Cleanroom Precision HVAC Cascade Differential Pressure Automation
  • WFI & Purified Water Circulation Loop Conductivity & Ozone Controls
  • Tablet Press, Granulation & Fluid Bed Dryer PLC Automation

Energy Solutions

  • Cleanroom Chiller Plant Variable Flow Optimization
  • Pure Steam Generator & Autoclave Steam Utility Profiling

Reliability & Inspection

  • Lyophilizer Refrigeration Compressor Vibration Telemetry
  • High-Shear Mixer & Homogenizer Mechanical Seal Monitoring
  • Cleanroom AHU Duct & Wall Thermal Insulation Imaging
  • Sanitary Stainless Steel Orbital Weld Borescope & NDT Inspection
Control System Topology

Typical Control Architecture

Redundant Siemens S7-1500 with WinCC Professional SCADA, audit trail database, and SAP ERP batch integration.

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