Pharmaceutical-grade purified water is produced in compliance with international pharmacopeia standards, including the Chinese Pharmacopoeia (CP), United States Pharmacopeia (USP), and European Pharmacopoeia (EP). These purified water systems typically rely on multi-stage filtration and membrane-based purification technologies, ensuring consistent water quality for drug production, laboratory use, and equipment rinsing. We offer complete system configurations tailored to specific user needs, covering everything from engineering design and equipment selection to automated control and validation support.
Our purified water production systems are designed according to the quality of the incoming water, required water standards, and the specific conditions of each project. WEMAC offers both customized and standardized solutions. Depending on the configuration, the pure water generation system can deliver water that complies with the quality specifications defined by the Chinese (CP 2020), United States (USP 43), and European (EP 10) Pharmacopoeias.
Note: Each pharmaceutical water system is custom-designed to meet the user requirement specification (URS) provided by the client. All photos and videos featured are from actual WEMAC projects.
When the conductivity exceeds the predefined threshold, the purified water system redirects the water back to the intermediate tank to maintain water quality before entering the next stage.
If the conductivity remains within acceptable limits, the water is delayed and sent to the purified water storage tank, ensuring consistent quality without premature transfer.
Uses first-pass permeate to flush the reverse osmosis membranes. The intermediate tank acts as both the starting and return point for the cleaning cycle.
Our purified water system includes a pretreatment unit, raw water storage tank, primary filtration section, and a purified water storage tank. Each section is integrated to ensure reliable water quality and smooth system operation from the initial stage to final output.
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