Can the system produce room-temperature WFI?

Yes. The membrane purification process can produce WFI at controlled low temperature without the high-temperature evaporation and condensation process used in conventional distillation.

Can Cold WFI be used for injectable production?

The system can be designed for pharmaceutical applications requiring WFI. The final process, specifications and validation should be confirmed according to applicable pharmacopoeial and regulatory requirements.

Can the system be customized?

Yes. Capacity, RO/EDI/UF configuration, storage tank, distribution loop, sanitization method, control system and documentation package can be customized according to the customer's URS.

What capacity is available?

The standard configuration can cover approximately 500-10,000 L/H, with other capacities available according to project requirements.

Can you provide qualification documents?

Yes. P&ID, drawings, material certificates, welding records, FAT/SAT and DQ/IQ/OQ/PQ documentation can be provided according to the project.

20000L/H Membrane-Based Water for Injection (WFI) Plant

Name: 20000L/H Membrane-Based Water for Injection (WFI) Plant
Brand: Shandong Eagle Pharma Machinery Co., Ltd.
SKU: 2190053612

Shandong, ChinaShandong Eagle Pharma Machinery Co., Ltd.

US$80,000.00

1 Piece

Product profile

Customization

Available

Application

Pharmaceutical Industry

Capacity

20000 L/hr

Model NO.

20000L/H

Certification

CE, FDA, GMP, ISO

Control System

Fully Automatic

Treatment Process

Electrodeionization, Filtration, Reverse Osmosis, Softening, Ultrafiltration

Warranty of core components

One Year

Product Type

Membrane Wfi Plant

Water Quality

Wfi

Purification Technology

RO + EDI + UF

Feed Water

Purified Water

Design Standard

GMP / USP / Ep / CHP

Membrane Technology

Ultrafiltration

Installation

Modular / Compact Design

Transport Package

Wooden

Specification

PW-20000

Trademark

WEMAC

Origin

China

HS Code

8419409090

Production Capacity

One Piece / Month

Key features

Up to 70% Energy Saving Membrane-based purification without a traditional steam-consuming distillation stage. The system produces room-temperature WFI and can reduce cooling and heat-exchange ene

Dual Endotoxin Barrier Double-Pass RO + EDI + 6,000-10,000 Da UF provides multiple purification and endotoxin-control barriers.

WFI Quality Control Designed around applicable EP, USP and ChP WFI requirements, with online conductivity, TOC, temperature and other critical parameter monitoring.

Room-Temperature WFI on Demand Produces WFI at controlled low temperature without requiring a downstream cooling stage, making it suitable for temperature-sensitive pharmaceutical processes.

Compact Skid-Mounted Design Modular skid-mounted construction requires less installation space and can be adapted to both new pharmaceutical facilities and existing plant upgrades.

Company profile

High Repeat Buyers ChoiceMulti-language PioneerQuality AssuranceFull Customization

Shandong Eagle Pharma Machinery Co., Ltd.

Shandong, China

Business Type: Manufacturer/Factory, Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service AvailableAverage Response Time: ≤3.15h

AI-Powered supplier vetting

SummaryThe supplier is identified as a trading company with a broad technical, equipment, software, and engineering-related business scope. It demonstrates professional technical R&D positioning, 3D software design, ODM, OEM, and multiple customization options. Quality and service procedures are partly established, including inspection instructions, complaint handling, supplier assessment, and corrective-action records. However, the supplier has only one quality inspector, has exported for one year, lacks raw-material traceability labels and written quality records, and has no overseas warehouse or showroom. Innovation evidence is mixed because no new products were reported in the past year and no SDK is available. Financial information is present only as year references, without sufficient evidence to assess credibility.

Supplier typeThe supplier is explicitly classified as a Trading Company. Its stated scope covers technical services, technology development, equipment sales, software development, IoT services, industrial engineering design, and equipment repair, indicating a technically oriented trading and service business rather than a clearly documented manufacturer.

After-Sales capabilityThe supplier has documented and followed procedures for complaint handling, supplier service-capability assessment, and corrective/preventive actions, and it reports in-stock service capability. However, it lacks overseas warehouse and showroom capabilities, so the evidence supports structured service handling but not comprehensive overseas support.

R&D capabilityThe supplier reports professional technical R&D capability, 3D software design, ODM services, and OEM services for popular brands. Counterbalancing this, it reported no new products during the past year and has no available SDK, so the evidence supports design and development services but not strong recent product innovation.

Customization capabilityThe supplier explicitly provides customization from samples, full customization, and customization from customer designs. It also offers 3D software design and ODM services, providing clear evidence of broad customization capability.

Product Q&A

Q:What is Cold WFI?

Cold WFI, also known as Membrane WFI, is Water for Injection produced using membrane technologies such as RO, EDI and UF rather than relying on a traditional thermal distillation stage.

Q:Does the system require a traditional WFI distiller?

No. The membrane process does not require a conventional multi-effect or vapor-compression distiller.

Q:How much energy can be saved?

The membrane process can provide up to 70% energy saving compared with suitable conventional WFI configurations. Actual savings depend on system capacity, existing utilities, raw water conditions and sanitization requirements.

Q:How does UF control endotoxins?

UF provides a physical barrier that can retain high-molecular-weight contaminants, microorganisms and endotoxin-related substances.

Q:What UF membrane specification is used?

A typical configuration uses a molecular weight cut-off of approximately 6,000-10,000 Da. The final UF specification is selected according to the process design and validation requirements.