A hospital operates a system for the central compressed air supply for medical compressed air. As part of the quality assurance and monitoring of the manufacturing process of the "air for medical use", EXCO validates the manufacturing process and qualifies systems and equipment according to current GMP, customer and normative requirements.
Tasks and implementation
- Requirements specification
- Functional detailed specification
- GMP validation/qualification plans
- GMP risk analysis
- Qualification (DQ, IQ, OQ, PQ)
- Process validation (PV)
- Validation and qualification report
- Traceability matrix
- Supplier qualification
- Accompaniment of FAT and SAT acceptance phases
Client benefits
- Achieving quality objectives: Measurements with electrochemical sensors and recordings and archiving of the measurement data mean the customer receives valid statements about their system’s conformity.
- Controlling suppliers: Supplier qualification ensures that the system and the equipment used are suitable in accordance with GMP guidelines.
- Estimating risks: The systems and equipment are qualified/validated prospectively using a risk-based approach. This qualification and validation are integral parts of the product life cycle.
- Training employees: EXCO provides employee training and external company training to ensure skills are transferred.
Client
Healthcare facility/Manufacturer of medical compressed air
