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

Cleanrooms within hospital facilities 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 disinfection procedures, to achieve an exceptionally low microbial load. By providing a st