Clean Room Testing and Adjustment are specialized processes used to ensure that controlled environments, such as clean rooms, meet stringent cleanliness and contamination control standards necessary for their intended use. These environments are critical in industries like pharmaceuticals, biotechnology, and semiconductor manufacturing, where even minute levels of particulate contamination can compromise product quality and safety.

Testing in clean rooms involves measuring and evaluating various environmental parameters to ensure they adhere to the specific standards required for the clean room's classification. Key parameters tested include particle count (size and concentration), temperature, humidity, air pressure, and airflow patterns.

Adjustment refers to the process of fine-tuning the clean room’s environmental control systems to achieve and maintain the desired conditions. This includes adjusting the air handling systems to control particles, as well as modifying temperature, humidity, and pressure controls to maintain strict environmental conditions. Adjustments are made based on the outcomes of the testing phase to ensure all parameters meet the specified cleanliness standards.

Overall, Clean Room Testing and Adjustment ensure that these critical environments are properly set up and maintained to support the high-quality production and research activities that depend on them. Regular testing and adjustment are essential to comply with industry regulations and to prevent contamination that could lead to significant financial loss and reputational damage.