The "Standards for the Quality Management of Pharmaceutical Production (2010 Revision)" was reviewed and approved by the Ministry of Health at its executive meeting on October 19, 2010. It is hereby issued and will be implemented on March 1, 2011.

Process water is indispensable in the production process of many medical device products, and its preparation, detection, storage, and other processes that affect the quality of process water directly or indirectly affect the quality of medical device products.Process water used in the medical device industry has some unique characteristics due to the characteristics of medical device products and their production processes.

The "Good Manufacturing Practice for Pharmaceutical Products (2010 Revision)" has been applied to the pharmaceutical water system, and has gradually grown into a well-known water equipment manufacturing and system solution provider.