As part of our regular after-sales service, we deploy the most efficient methodology to ensure the highest performance of our Air Filtration Systems. AFi validation service provides the environmental conditions of the clean rooms that have been defined in the HVAC order from the user process requirements.

Regular validation minimizes product defects, costly downtime and hence increases productivity. AFi validation team provides independent customer-friendly Clean Room validation and Clean Room Certification Service with sophisticated calibrated instruments.

Air quality is critical especially in industries like pharmaceuticals, semiconductor, aerospace, research facilities, laser and optic industries etc. When a clean room has just been built it must be tested to ensure that it is meeting the regulatory requirements given in ISO 14644-1. Validation of a new clean room follows a specified lifecycle. The life cycle comprises five phases each of which accomplishes particular tasks to control variation in the modular environment. It starts off with the design control phase and ends with monitor and control. Changes to equipment and control factors after the clean room has been validated, are grounds for Clean Room Re-validation.