Maintaining a consistent and verifiable level of purity in a cleanroom environment is paramount for sensitive manufacturing processes across various industries, including pharmaceuticals, electronics, and microfabrication. ISO specifications provide a globally recognized system for classifying these spaces based on the concentration of airborne deb

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 cleaning procedures, to achieve an exceptionally low microbial load. By providing a steril