The production and economic survival of pharmaceutical/biopharmaceutical/medical device manufacturers largely depend on the safety of the finished product. Therefore, it is necessary to know the potential sources of pollution, and pollution control sources require clean rooms.
A major design aspect of a cleanroom is to extract each manufacturing process, identify key work steps, and classify the corresponding cleanroom categories for manufacturing.
For pharmaceutical/biopharmaceutical/medical device production cleanrooms, it usually ranges from ISO 5 to ISO 7. Through the experience of our professional team, we will provide comprehensive cleanroom solutions.