Laboratory Central Pure Water System (Dual-Module Integrated)

The entire system is made of SUS304L or SUS316L all stainless steel material, with polished inner walls and no dead corners design, fully meeting the strict requirements of the pharmaceutical industry for corrosion resistance and cleanliness. The disinfection methods are flexible and optional, including activated carbon pasteurization, CIP cleaning system, distribution system ozone sterilization, distribution system pasteurization, and distribution system pure steam sterilization. They can be configured according to your process requirements and production arrangements to effectively control microbial growth.

The system is based on functional units such as pretreatment, oxidation disinfection, multi-media filtration, RO reverse osmosis, UV disinfection, EDI continuous deionization, and storage and export. We first conduct a URS requirement analysis to understand your water standards (purified water/injection water), water production, raw water quality, etc., and then tailor the optimal combination solution for you. For example, conventional formulations can use RO+EDI for water, while biopharmaceuticals with extremely high water quality requirements can use multi-stage RO+EDI+UV+purification processes to ensure the optimal balance between performance and cost.

Absolutely possible. Our system is designed strictly in accordance with the latest Chinese, American, and European pharmacopoeia water quality standards, and meets the requirements of GMP, FDA, cGMP, and ISPE/FDA guidelines. More importantly, we provide full process validation services, including URS requirement analysis, DQ, FAT, SAT, IQ, OQ, PQ and other complete validation documents, to ensure that every functional unit has been strictly confirmed, providing strong guarantees for you to smoothly pass the audits of domestic and foreign drug regulatory departments.