In the pharmaceutical/bio-pharmaceutical/medical device production and economical survival of the manufacturer, depend heavily on the safety of the finished product. It is therefore needed to know a potential source of contamination, which a cleanroom is required for the source of contamination control.
One main design aspect for the cleanroom is to extract each manufacturing procedures, identifying the crucial working steps, and hence, classify the corresponding cleanroom class for manufacturing.
For pharmaceutical/bio-pharmaceutical/medical device production cleanroom, it usually specified from ISO 5 to ISO 7. Through experiences of our expertise team, a comprehensive solution for cleanroom classification will be given.