Touch screen pharmaceutical RO Unit Purified ultra pure edi water system

Purified Water System

Main description

This system is designed for the purified water project. Design the water source to master the worst water quality, and the production capacity is designed according to requirements.

According to the different products, the effluent quality of the system meets the water requirements.

The design water source is based on municipal water.

The system is designed according to the user's raw water quality and the water quality requirements.

The system configuration and settings can fully meet the requirements of water inlet conditions, with the principles of automatic, energy saving, simple operation, environmental protection and safety, and ensure the system can run stably for a long time.

The purified water system processes involve pretreatment via softening and microfiltration stage followed by a reverse osmosis stage and a final demineralization via the patented EDI module. This process technology meets current USP and European Pharmacopoeia requirements in a safe and reliable way. Each system is pre-qualified before shipment and undergoes a full functional FAT test at our factory.

Main performance and features

      (A).  TOC<100ppb

      (B) . Conductivity <0.5us/cm

      (C) . Microorganism<100CFU/ML

      (D) . Endotoxin <0.25EU/ml

      (E) . Nitrate<0.06ppm

      (F) . Heavy metal <0.1ppm

(1)According to the water quality and customer’s requirements, the two stage RO or RO+EDI configurations are provided.

(2)Modular design, compact structure, convenient installation and operation

(3)Double-stage softener series operation, no spare equipment dead water risk.

(4)Multi-channel diaphragm valves replace multiple individual valves, reduce dead corners, facilitate emptying, reduce the amount of verification documents and reduce the number of welds.

(5)The wastewater discharge line is integrated into the frame, with less pipe and less weld, the optimum separation of purified water and waste water.

(6)The sampling points at each stage of the system are at their best, easy to maintain and sample.

(7)Frequency conversion control, dual pipeline water supply, non-water state low –frequency circulation, no intermediate water tank. Reduce the risk of microbial development.

(8)RO unit is developed regularly and the system can be chemically sterilized or pasteurized.

(9)Full automatic operation, unattended, remote control

(10)The automatic control system meets the requirements of the CFR part 11 and GAMP5 to meet the FDA and EU cGMP requirements.

(11)Provide standard and extended documentation according to customer requirements to meet FDA and EU cGMP verification requirements.

Techncial parameters

Technical parameters