Validation for cleanrooms and operating rooms (OR)

Egemin Automation has the experience and knowledge to support you in all your validations of both cleanrooms and operating rooms.

Cleanrooms, production areas and operating rooms

Egemin Automation will help you check whether your cleanrooms, production areas and operating rooms meet the international regulations (EU, FDA, ISO) or GAMP. We will gladly work out a programme for you for periodic control or (re)qualification of your cleanrooms.

• Air volumes
• Pressure differences
• Filter integrity
• Air velocity
• Particle classification
• Microbiological sampling
• Air current patterns: Visualisation and registration
• Recovery time
• Temperature
• Relative humidity
• Light
• Sound

Advanced measuring instruments

By means of a pre-approved protocol we analyse whether your cleanroom complies with the acceptance criteria. After the measurement the end report is discussed with you in detail; in consultation with the responsible services or suppliers if desired. This report also contains recommendations on how to approach any comments or deviations.