Irish Power & Process can facilitate all of your validation requirements in both the Medical device and the pharmaceutical industry. Validation is the practice of ensuring that a product, process or equipment conforms to defined needs, requirements, or specifications under predefined operating conditions. The purpose of Validation is to ensure that a quality product can be reproduced to a pre-defined standard consistently.
Some of our Validation Services include IQOQ of Data Acquisition equipment, Thermal Validation of Lab and Production equipment.
Full Service Commissioning & Qualification packages for Instrumentation and Controlled environments such as:
- Biological Safety Cabinets
- LAF Workstations
- PCR Hoods
- Fume Hoods
- Cleanrooms
