Maintaining a consistent and verifiable level of sanitation in a cleanroom environment is paramount for precise manufacturing processes across various industries, like pharmaceuticals, electronics, and microfabrication. ISO standards provide a globally recognized structure for classifying these spaces based on the concentration of airborne matter.

Cleanrooms within hospital settings are paramount in maintaining sterility and minimizing the risk of healthcare-associated infections. These specialized rooms utilize stringent protocols, including regulated airflow, HEPA filtration systems, and meticulous cleaning procedures, to achieve an exceptionally low microbial load. By providing a sterile