Industry Architecture
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 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.
Partner With Nexus Dynamics
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