cGMP Pharmaceutical Purified Water Treatment / RO EDI Water Purification System

Name: cGMP Pharmaceutical Purified Water Treatment / RO EDI Water Purification System
Brand: Shanghai Iven Pharmatech Engineering Co., Ltd.
SKU: 1927262301

Shanghai, ChinaShanghai Iven Pharmatech Engineering Co., Ltd.

US$50,000.00-250,000.00

1 Piece

Product profile

Application

Biotechnology Industry, Chemical industry, Forensic Science, Pharmaceutical Industry, Industry

Capacity

100 Gallon

Certification

Model NO.

customized

Control System

Semi-automatic

Treatment Process

Chlorination, Electrodeionization, Ozonation, Reverse Osmosis, Softening, UV Disinfection

Warranty of core components

1 Year

Max Working Pressure(MPa)

10000 MPa

Volume

1000L-10000L

Height

2000-3900mm

Diameter(mm)

900-2000

Diameter

900-2000mm

Core Components

Pump, PLC

Weight

Customized

Function

Purified Water Preparation

Keywords

RO EDI Water Treatment Machine

OEM

Acceptable

Type

Purified Water Generation System

Filter Material

RO Reverse Osmosis

Salt Rejection Rate

99.5%

Transport Package

Wooden Case;

Specification

customized

Trademark

IVEN

Origin

China

Production Capacity

Customized

Company profile

Years of Export ExperienceLow MOQPatents AwardedProduct Certification

Shanghai Iven Pharmatech Engineering Co., Ltd.

Shanghai, China

CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedCustomization Options: Customization from Samples, Customization from Designs, etc. CertifiedExport Year: 19 Years CertifiedNearest Port: Shanghai PortAverage Response Time: ≤1.80h CertifiedTerms of Payment: LC, T/T, D/P, etc.

AI-Powered supplier vetting

SummaryThe supplier is a combined company offering pharmaceutical and medical production equipment, including vial, ampoule, prefilled syringe, oral liquid, tablet, capsule, visual inspection, packaging, and logistics solutions. It provides extensive customization and integrated services such as process design, equipment selection, installation, commissioning, and validation. Export activity is substantial, with 71%–90% of sales from exports and 19 years of export experience. Quality assurance, ISO9001:2015 certification, CE capability, manufacturing contracts, and finished-product inspection instructions are documented strengths. However, the supplier lacks in-stock, overseas warehouse, overseas showroom, overseas agent or branch capabilities, and has no written procedures for service assessment, corrective actions, or complaint handling. R&D evidence is limited: no SDK, no new products in the past year, and no ODM or major-brand OEM services. No specific customer cases are provided.

CertificationsThe supplier reports an ISO9001:2015 certificate and CE certification capability, providing explicit evidence of quality-management and product-compliance credentials. However, the slices do not specify the scope, validity period, or products covered by these credentials.

After-Sales capabilityThe supplier lists installation, commissioning, validation, maintenance, debugging, repair, training, and integrated consulting services, and provides equipment installation-related offerings. Nevertheless, it has no overseas agents or branches, no overseas warehouse or showroom, and no written procedures or records for complaint handling, service assessment, or corrective and preventive actions, indicating an operational weakness in documented after-sales management.

R&D capabilityThe supplier has customization-oriented R&D services, but reports no available SDK, no new products during the past year, no ODM service, and no OEM service for popular brands. These explicit limitations indicate weak evidence of current product innovation and platform development.

Production capacityThe supplier covers multiple pharmaceutical equipment production lines, including vial and ampoule, prefilled syringe and cartridge, oral liquid, tablet and capsule, inspection, packaging, and logistics systems. It has valid manufacturing contracts with each affiliated subcontractor, follows finished-product inspection instructions uniformly, and reports quality assurance, although no quantitative production-capacity data is provided.

Customization capabilityThe supplier explicitly offers customization from samples, designs, full customization, minor customization, and flexible customization. Its integrated solution includes process design, conceptual and construction design, equipment selection, model customization, installation, commissioning, and validation, demonstrating broad customization coverage.