Is a highly regulated process that involves the production of sterile drugs under controlled conditions to ensure the safety and efficacy of the drugs. The manufacturing process takes place in a sterile environment, where every aspect of the production process is designed to minimize the risk of contamination. To achieve this, environmental monitoring plays a crucial role in ensuring that the cleanroom conditions meet the required standards.

Environmental monitoring in aseptic pharmaceutical manufacturing involves regular testing of the air and surfaces in the cleanroom to detect the presence of any contaminants that could pose a risk to the production process. The cleanroom is equipped with specialized air filtration systems, and workers must follow strict protocols to prevent contamination.