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Brand Name : CHONGYANG
Model Number : CY-WFI-300Liter/Hour
Certification : ISO ,CE
Place of Origin : China
MOQ : 1
Price : Negotiation
Payment Terms : L/C, T/T
Supply Ability : 100 Sets/Months
Delivery Time : With 30-40 Days
Packaging Details : According to export standard
Material : SS316L
Stages : Double RO +EDI+ Ultrafiltration
Valve : Diaphragm Valve
Pump : Grundfos, CNP
Conductivity : 1.3μS/cm
Requested Feed Water : Purified Water System
Product Name : Ultrafiltration WFI Water
Standard : FDA,USP,cGMP,GMP
Pipeline Material : BPE,SS
Capacity : 100L/H -10,000L/H
Product Overview: The Membrane-Based WFI System is designed for pharma Water for Injection production using double-pass RO, EDI and ultrafiltration technology. It provides stable water quality, lower energy consumption and GMP-compliant operation for modern pharmaceutical manufacturing.
This system is widely used in pharma manufacturing, biotechnology production, sterile preparation, laboratory research and medical industries where high-purity Water for Injection is required for injection, cleaning and process water applications.
| Item | Specification |
|---|---|
| Capacity | 100–10,000 L/H |
| Conductivity | ≤1.1 µS/cm @25°C |
| TOC | ≤500 ppb |
| Endotoxin | ≤0.25 EU/ml |
| Bacteria | <10 CFU/100 ml |
| Material | SS316L, internal Ra <0.4 μm |
| Control System | PLC + HMI, or Schneider optional |
The system includes multimedia filter, activated carbon filter, water softener, double-pass RO membranes, EDI module, ultrafiltration membrane for endotoxin removal, sanitary pumps, UV sterilizer, ozone system, SS316L storage tank and automatic PLC control system.
Our membrane-based WFI systems have been applied in pharmaceutical factories in Southeast Asia, the Middle East and Europe, helping customers achieve stable WFI production, GMP validation and continuous operation.
The system is designed according to GMP, FDA, USP, EP and WHO requirements. Optional IQ/OQ/PQ validation support and complete documentation can be provided for audit and compliance needs.
Q: Is membrane-based WFI acceptable under GMP?
A: Yes. It can be accepted with proper system design, validation and water quality control strategy.
Q: What are the advantages compared with distillation?
A: Lower energy consumption, compact design, faster startup and flexible operation.
Q: Can the system be customized?
A: Yes. Capacity, materials, control system and validation documents can be customized.


FAQ:
1.Question: Which process do you adopt ?
Answer:Usually we will be according to what your raw water quality and your requested water requirement .
2. Question:Can you customize For me?
Answer :Yes. We can manufacture according your requirement , we can even design appearance of equipment .
3.Question: What standards is the Pharmaceutical Purified Water System ?
Answer: Usually there are five standards in this pharmaceutical industry , FDA,cGMP ,GMP ,USP, Japanese .
4.Question:How long is the Delivery time ?
Answer: Usually the delivery time is 35 -40 Days .
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Membrane-Based WFI System Images |