Pharmaceutical Automation System
We provide validated pharmaceutical automation solutions designed to ensure product quality, regulatory compliance, and consistent process control across manufacturing operations.
Our systems integrate process equipment, cleanroom instrumentation, and control platforms to support GMP-compliant and data-integrity-focused production.
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Scope of Work
Process automation design, PLC & SCADA programming, cleanroom integration, validation support, commissioning, and operator training.
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Automation Design & Engineering
Control philosophy, batch control logic, recipe management, I/O mapping, alarm philosophy, HMI design, and technical documentation.
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Factory Acceptance Test (FAT)
Controlled testing with documented protocols including PLC simulation, batch sequence verification, alarm handling, and audit-ready records.
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Site Acceptance Test (SAT)
On-site commissioning with IQ/OQ support, system integration testing, and performance validation under actual production conditions.
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Pharma Automation Solutions
- PLC, SCADA & DCS Systems
- Batch Process Automation
- Clean-in-Place (CIP) & Sterilize-in-Place (SIP)
- Environmental Monitoring Systems (EMS)
- Packaging & Serialization Automation
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Standards & Compliance
Designed to comply with GMP, GAMP 5, FDA 21 CFR Part 11, EU Annex 11, and applicable IEC & ISO standards.
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Applications
API manufacturing, formulation, sterile production, filling lines, packaging systems, and utility automation.
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Key Benefits
- Regulatory-compliant automation
- Improved batch consistency and traceability
- Enhanced data integrity and audit readiness
- Reduced contamination risk
- Scalable systems for future expansion