HOP YUEN INDUSTRIAL LIMITED

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.

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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. 

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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.