ChP/USP/EP/GMP 300L/H Deionized Water System For The Raw Water Pretreatment Of Preparing WFI
Place of Origin | Shenzhen,Guangdong |
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Brand Name | HJW |
Certification | ISO 14001,ISO 9001,CE,EPA,ChP,USP,EP,GMP |
Minimum Order Quantity | 1set |
Price | ≤US$2105 |
Packaging Details | export standard wooden case |
Delivery Time | 1-7working days(depand on raw materials stocking) |
Payment Terms | L/C,D/P,T/T,Western Union |
Supply Ability | >300sets/month |

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xCapacity | 30L/H(Customizable) | Pipes/Tanks Material | 316L Stainless Steel (Ra ≤ 0.6 μm) Or PVDF |
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Disinfection Methods | Pasteurization (80–85°C Cycle) Or Ozone Sterilization | Monitoring System | Online Conductivity Meter + TOC Analyzer |
Documentation System | DQ/IQ/OQ/PQ Validation Documents (core Items For EMA/FDA Audits). | Microorganism | ≤100 CFU/mL |
Highlight | 300L/H Deionized Water System,GMP Deionized Water System,USP deionized water machine |
I. Overview
Deionized water (DI water) equipment plays a central role in the raw water pretreatment stage of preparing water for injection (WFI), and its quality directly determines whether the final WFI meets the stringent standards of national pharmacopoeias.
The irreplaceable role of DI water in WFI preparation: The irreplaceable role of DI water in WFI preparation, economic barriers, the cornerstone of sterility assurance, and the core of green transformation.
System selection principles:
Choose CEDI-type DI water equipment (no chemical regeneration) + 316L stainless steel high-temperature circulation system + online TOC/conductivity monitoring, and reserve an inlet interface for the distillation unit to meet FDA/EMA dynamic production review requirements
II.Main Process
Raw Water→Pretreatment→RO Reverse Osmosis→CEDI →PW Storage Tank→Distillation/Pure Steam→WFI
III.DI Water Equipment Core Section (PW Preparation)
Step | Measures | Parameters | |||||
Enhanced Pretreatment | Ultrafiltration (UF, 0.03 μm): Remove colloids/microorganisms | SDI < 3; TOC < 50 ppb; Hardness < 1 ppm | |||||
Activated carbon: Adsorb organics | |||||||
Softener: Prevent scaling | |||||||
Dual Desalination | Primary/Secondary RO: Desalination rate > 99% | Produced water conductivity < 5 μS/cm; Resistivity 5–18 MΩ·cm | |||||
CEDI: Deionization | |||||||
Microorganism Control | 254 nm UV disinfection | Microorganisms < 10 CFU/mL | |||||
Storage tank: Heat preservation circulation (>80°C) |
IV.DI Water System Critical Process Points (CPP)
Risk Point | Control Measures | Pharmacopoeia Compliance Basis | |||||
Microbial Growth | Storage tank/pipeline > 80℃ circulation + Ozone disinfection | USP <1231>: High - temperature or sterile filtration recommended | |||||
TOC Exceedance | RO membrane + CEDI + Activated carbon three - stage interception | EP 9.0: TOC detection is mandatory | |||||
Endotoxin Source | UF ultrafiltration (Retention of substances > 10 kDa) | ChP 2020: Endotoxin only tested for final products | |||||
Resistivity Fluctuation | Online conductivity meter + Automatic drain valve | GMP: Real - time monitoring of key parameters |
V.Here is a guideline for you to get a proper quotation
Tell us the raw water/source of water(tap water, well water, or sea water, etc)
Provide water analysis report(TDS , conductivity, or resistivity, etc)
Required production capacity( 5m³/H, 50m³/H,or 500m³/H, etc)
What's the pure water used for( industrial,Food and Beverage,or agriculture, etc )