Regulated Automation for Pharma & Biotech
In pharmaceutical manufacturing, verifiable compliance is as critical as the physical process itself. We provide end-to-end automation solutions strictly adhering to Good Manufacturing Practices (GMP). From conceptual design to site commissioning, our engineered systems guarantee absolute data integrity. We utilize a structured GAMP 5 approach to ensure that every control sequence and logic block is traceable, tested, and validated.
Typical Scope
- Bioreactor Control
- Media Preparation
- Extraction & Purification
- WFI (Water for Injection) Systems
- Cleanroom HVAC Integration
What You Get
- Standardized Batch Execution (ISA-88)
- Automated Electronic Batch Recording
- Comprehensive Lifecycle Documentation
Compliance, Safety & Reliability
- GxP/CSV compliant software architecture
- Execution of exhaustive FAT/SAT protocols
- Secure audit trails & 21 CFR Part 11 adherence
How we execute
Discover our rigorous engineering methodology.
