Engineered for Regulatory Compliance and Cleanroom Integration
Axium Process supplies pharmaceutical-grade CIP systems designed to meet the stringent hygiene, traceability and validation requirements of GMP-regulated environments. Each system is developed in accordance with ASME BPE, GAMP 5 and FDA guidelines to ensure full compliance and audit readiness.
These systems are supplied with full documentation, including material certification, validation protocols and traceability dossiers. Where required, systems can be supplied skid-mounted with integrated steam-in-place (SIP) functionality for terminal sterilisation.
Key Features
- Hygienic design with orbital welding and electropolished finishes
- Sanitary pumps, valves and instrumentation
- Cleanroom-compatible components and connections
- Pre-validated designs available with complete lifecycle documentation
- Supplied with IQ/OQ documentation and FAT/SAT support
Pharmaceutical CIP systems are available with advanced automation, full batch traceability and remote data access to support regulatory inspections and production integrity.