Pharmaceutical Water Plant

USP/EP grade purified water generation systems meeting stringent pharmaceutical industry compliance and validation requirements.

How It Works

Our pharmaceutical water systems are designed to meet the exacting standards of the pharmaceutical industry for Purified Water (PW) and Water for Injection (WFI) as per USP, EP, and IP pharmacopoeia. The system typically consists of a pre-treatment section (softener, carbon filter), double-pass RO, EDI (Electrodeionization), UV sterilization, and a storage & distribution loop with CIP/SIP capability. All contact surfaces are electropolished SS 316L, and the system is supplied with complete IQ/OQ/PQ documentation for regulatory validation.

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Technical Specifications

Water Grade USP Purified Water / WFI
Conductivity < 1.3 Microsiemens (at 25°C)
TOC < 500 PPB
Endotoxin (WFI) < 0.25 EU/ml
Construction SS 316L Electropolished
Capacity 500 - 10,000 LPH

Why Choose Our Solution

01

Pharmacopoeia Compliant

Systems designed to meet USP, EP, and Indian Pharmacopoeia standards for purified water.

02

Double Pass RO + EDI

Two-stage RO followed by EDI produces chemical-free, consistently high-purity water.

03

SS 316L Construction

All product contact surfaces in electropolished SS 316L for zero contamination risk.

04

Loop Distribution

Validated distribution loop with sample points, TOC monitoring, and continuous recirculation.

05

CIP/SIP Ready

Integrated Clean-In-Place and Sterilize-In-Place systems for GMP compliance.

06

Full Documentation

Complete IQ/OQ/PQ validation protocols and documentation for regulatory audit readiness.

Applications

Pharma ManufacturingAPI ProductionFormulation PlantsBiotech LabsMedical DevicesCosmetics IndustryR&D Laboratories

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Our engineers will assess your requirements and provide a customized solution with competitive pricing.