Validation & Commissioning
Validation and commissioning are critical processes in ensuring that systems and equipment in regulated environments, such as pharmaceuticals, biotechnology, and healthcare, operate according to predefined specifications and comply with industry standards.
Innixi Solutions provides calibration services that adhere to DQ, IQ, OQ, and PQ protocols. Our validation services for Clean Rooms and Clean Room Equipment i.e. LAF, that comply with international standards ISO, EUGMP, CGMP, ISPE, WHO and include comprehensive test certificates and documentation. The details of these services are outlined below:
- Air velocity measurements, balancing, and calculations of air changes per hour
- Simulation and visualization tests for airflow patterns
- Debugging services to identify sources of contamination
- In situ DOP leak testing and particle monitoring
- Induction leak testing
- Recording of temperature, humidity and pressure levels