500lph Pharmaceutical Purified Water System Reverse Osmosis Machine Pw Water Purifier GMP USP

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500lph Pharmaceutical Purified Water System Reverse Osmosis Machine Pw Water Purifier GMP USP

Customization:	Available
Certification:	ISO9001, CE, ISO14001
Salt Rejection Rate:	99.5%

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Product Description

Basic Information

Model NO.MOLPW

ApplicationSolid & Liquid Preparations

Capacity3000L/H

Power Supply380V, 50Hz (Customizable)

TechnologyDouble Stage RO + EDI

DisinfectionHeat Disinfection

StandardGMP, USP, FDA

Warranty1 Year

Packaging & Delivery

Package Size500.00cm * 150.00cm * 200.00cm

Gross Weight1000.000kg

Transport PackageWooden Box

Product Description

Pharmaceutical purified water system is designed to comply with GMP and USP standards.

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Raw Water Treatment: Pasteurization applied to activated carbon filters; three-stage pretreatment for removal of impurities.

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Reverse Osmosis + EDI: Energy-saving design with water recycling (recovery rate ≤30%).

✓

Quality Monitoring: Real-time conductivity monitoring (RO product ≤5 μS/cm, EDI product ≤1μS/cm) and online TOC monitoring (≤500 ppb).

Technical Specifications

Technical Parameters
Product Name	Pharmaceutical Purified Water Systems
Material	SS304 / SS316L
System Type	Fully Automated Generation System
Purification Technology	Double stage RO+EDI
Core Components	Pressure Vessel, High-Pressure Pump, PLC Controller, EDI Module
Control System	PLC + HMI (Automatic And Manual Mode)
Voltage	220V / 380V (Customizable)
Certification	ISO 9001, ISO 14001, ISO 45001, CE

Functional Advantages

◈ Advanced Purification Technology

Integration of cutting-edge RO and Electrodeionization (EDI) technology ensures ultra-pure water that exceeds pharmacopoeia requirements with a built-in safety margin.

◈ Intelligent Automation & Quality Control

PLC+HMI control system features automatic and manual modes with real-time monitoring and intelligent algorithms to maximize efficiency.

◈ Modular & Sanitary Design

Simplifies installation and maintenance. Components use pharmaceutical-grade stainless steel with a dead-leg-free design to prevent microbial growth.

Core Applications

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Solid Dosage Manufacturing: Tablets, capsules, granules, and powder formulations.

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Sterile & Injectable Support: Pre-treatment for WFI systems and sterile bulk manufacturing.

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API Production: Chemical reactions, washing steps, and solvent preparation in bulk drug substance production.

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QC Testing: Solution preparation and glassware rinsing in pharmaceutical laboratories.

Facility Showcase

Frequently Asked Questions

Q1: Is your system compliant with international regulatory requirements?

A: Yes, the system is fully compliant with international standards such as FDA, GMP, and WHO. We provide a complete DQ/IQ/OQ/PQ validation document package.

Q2: What documentation is provided after shipment?

A: We provide all original documents including Packing List, Commercial Invoice, B/L, and specific certificates as required by the client.

Q3: Can the product water indicators stably meet pharmacopoeia standards?

A: Yes, water production is stable and meets USP, EP, JP, and Chinese Pharmacopoeia standards for pharmaceutical water.

Q4: Do you arrange shipment for large-scale equipment?

A: Yes, for CFR or CIF terms, we arrange the shipment. For FOB terms, clients can arrange shipment via their own forwarders.

Q5: What installation and training services are provided?

A: We provide on-site or remote online guidance for installation, maintenance training in English, and 24/7 after-sales online support.

Q6: How does the energy-saving design work?

A: Our smart operational optimization reduces energy consumption by up to 30% through recycling concentrated water and utilizing efficient EDI modules.