The pharmaceutical and food industries along with medical device producers must follow the standardized Good Manufacturing Practice (GMP) for their Cleanrooms which establishes particular hygiene and cleanliness requirements.
Due to the complexity of the external environment, it is not easy to realize the actual cleanliness of Fab. The main sources of contamination are particles, metal elements and organic matter from personnel activities. Particles and metal elements from equipment operation. Particles, metal elements and organic matter from raw and auxiliary materials. Particles of oxidized organic matter from operating methods. And particles from the workshop environment. Of these, particulate matter accounts for about 37-70%, liquid particles for about 10-30%, and microorganisms for about 5-20%.
Food production depends upon the Clean Room to stop cross-contamination from happening. Enterprises need to address scientific approaches for designing and deploying contamination prevention systems as their main priority.
There are significant differences in the application of Clean Rooms in different fields, mainly in terms of cleanliness levels, control objects, design requirements and application standards. Their main differences are as follows:1. In addition to temperature, humidity, pressure and other environmen
Amber is a professional engaged in providing turnkey solution in a clean room project such as hospital operating room, ICU, ward, pharmaceutical, bio-lab and so on.
