SS316L Pharmaceutical Water System Pure Water System RO System

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SS316L Pharmaceutical Water System Pure Water System RO System

Customization:	Available
Application:	Biotechnology Industry, Chemical industry, Clinical Diagnosis, Energy & Mining, Food & Beverage Factory, Food Safety, Forensic Science, Pharmaceutical Industry
Capacity:	1000lph

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Product Description

📊 Basic Info.

CertificationCE, FDA, GMP, ISO

Control SystemFully Automatic

Treatment ProcessRO, EDI, UV Disinfection

MaterialSS304 + SS316L

DisinfectionHeat Disinfection

Production Capacity500 sets/Year

Package Size200.00cm * 180.00cm * 210.00cm

Package Gross Weight1500.00kg

💧 Product Description

Pharmaceutical Purified Water System, WFI Multi-effect Distiller, and Pure Steam Generator.

We provide comprehensive turn-key solutions for pharmaceutical water system projects, covering technical design, high-precision manufacturing, global shipping, on-site installation, and professional operational training.

📋 Technical Specification

No.	Unit	Parameter Information
1	Name	3000L/H Purified Water (PW) System
2	Model	MOLPW-3000L
3	Permeate Capacity	3000L/H @ 25℃
4	Feed Water	Municipal Tap Water
5	Pure Water Quality	Electrical Conductivity < 1.3μs/cm (Meets GMP, EP/USP)
6	Technology	Double Stage Reverse Osmosis + EDI Unit
7	Control Method	Automatic PLC Control (Manual override available)

🚀 Functional Advantages

✅ Advanced Purification Technology

Our systems integrate cutting-edge Reverse Osmosis (RO) and Electrodeionization (EDI) technology to consistently produce ultra-pure water that exceeds global pharmacopoeia requirements with a significant safety margin.

✅ Intelligent Automation

Equipped with a high-end PLC+HMI control system, the equipment offers real-time monitoring and intelligent algorithms to optimize operational parameters, maximizing efficiency while minimizing manual intervention.

✅ Modular & Sanitary Design

The modular construction simplifies installation and future expansion. All contact components are pharmaceutical-grade stainless steel with a dead-leg-free design to prevent microbial growth.

✅ Multi-Layer Safety

Features include advanced alarm systems, self-diagnostics, pressure relief valves, and abnormal water quality alerts to ensure continuous safe operation for critical processes.

✅ Energy Efficient Operation

Smart optimization reduces energy consumption by up to 30% compared to conventional systems. The EDI module significantly lowers operational costs and environmental impact.

✨ Key System Features

Raw Water Treatment: Pasteurization applied to pretreatment filters with three-stage removal of particles and impurities.
Energy-Saving RO+EDI: Concentrated water recycling (up to 30% recovery) and EDI return systems.
Precision Monitoring: Online conductivity monitoring (RO ≤5 μS/cm, EDI ≤1μS/cm) and TOC monitoring (≤500 ppb).
Sanitary Distribution: Pasteurization-ready distribution loops for total microbial control.

📸 System Showcase

❓ Frequently Asked Questions

What is the typical process flow of a pharmaceutical purified water system?

A typical PW system includes pretreatment (multimedia filtration, activated carbon, softening), followed by double-stage Reverse Osmosis (RO) and Electrodeionization (EDI), with a circulation loop featuring UV/Ozone sanitization.

Why is EDI preferred over mixed-bed ion exchange?

EDI avoids the need for chemical regeneration, reduces contamination risks, ensures stable water quality, and complies better with GMP requirements for continuous production.

What key quality parameters must be monitored?

Key parameters include electrical conductivity, Total Organic Carbon (TOC), microbiological count, pH levels, and endotoxin levels, adhering to USP, EP, or ChP standards.

What is the difference between Purified Water (PW) and Water for Injection (WFI)?

PW is used for non-parenteral products. WFI has much stricter limits for microbes and endotoxins and is typically produced through distillation or multi-effect evaporation.

How is microbial growth controlled in the distribution loop?

Microbial growth is controlled by maintaining continuous high-velocity circulation, using heat sanitization (pasteurization), installing UV sterilizers, and ensuring a dead-leg-free piping design.

How often does the system require maintenance?

Standard maintenance includes periodic filter replacements, RO membrane cleaning (CIP), and sensor calibration. Intelligent PLC alerts help notify operators when maintenance is due based on performance data.