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Hm Pharma Water System&, Formulation System Cleaning System
US$100,000.00-200,000.00
1 Piece

Product profile

Customization

Available

Application

Biotechnology Industry, Chemical industry, Clinical Diagnosis, Food & Beverage Factory, Pharmaceutical Industry

Capacity

5000 L/hr

Model NO.

HM PW

Certification

CE, GMP, ISO

Control System

Fully Automatic

Treatment Process

Chlorination, Electrodeionization, Filtration, Ozonation, Reverse Osmosis, Softening, Ultrafiltration

Warranty of core components

1 Year

Type

Pharmaceutical Water Treatment Equipment

Finished Dosage Form

Liquid

Precision

High Precision

Voltage

380V

Computerized

Computerized

Customized

Customized

Condition

New

Warranty

1 Year

After-Sales Service

Online, at Site

Transport Package

Seaworthy Packing

Specification

as required

Trademark

HM PHARMACHINE

Origin

Zhejiang China

Production Capacity

30 Per Year

Key features

Compliance with Global Standards: Meets EP, USP, WHO GMP, EU cGMP, and US FDA regulations for pharmaceutical water systems.
Advanced RO Technology: High-resolution infiltration RO system effectively eliminates salts, microbes, heavy metals, and pyrogens.
Energy-Efficient Distillation: Multi-effect distillation saves up to 77% water and 23% energy compared to traditional methods.
Zero Pollution EDI System: Continuous production with no wastewater or acid/alkali chemicals, ensuring stable high-purity water.
Stainless Steel Sanitary Design: Pipelines meet cGMP standards with stainless steel sanitary level construction for safe distribution.
Automated Control System: Siemens PLC and touch screen control with online conductivity monitoring for precise operation.
Versatile Water Applications: Suitable for purified water, WFI, pure steam, and various dosage forms including injectables and liquids.
Customized Manufacturing: Equipment is fully customizable in type, voltage, and precision to meet specific client requirements.

Company profile

HM Pharmaceutical Engineering & Project (Zhejiang) Co., Ltd.
Importers and ExportersYears of Export Experience
Business Type: Manufacturer/FactoryExport Year: 1999-03-18Nearest Port: SHANGHAI,CHINA, NINGBO ,CHINAAverage Response Time: ≤2.81hTerms of Payment: LC, T/T, D/P, etc.International Commercial Terms(Incoterms): FOB, CFR, CIF

AI-Powered supplier vetting

SummaryHM Pharmachine Group presents evidence of established manufacturing, export, and customization capabilities. It operates three production lines, has 6–10 quality-control staff, reports 11–20 years of R&D engineer experience, and has exported for 16 years to broad international markets. Its management-system certifications include ISO9001:2015, ASME, and GMP. Customization is offered from samples, designs, and through full customization, supported by CAD and PORTAL tools and documented R&D inputs, outputs, reviews, verification, and validation. However, important gaps remain: no approved-supplier list, written corrective-action or complaint-handling procedures, valid manufacturing-capacity contracts with related subcontractors, overseas warehouse or showroom capability, environmental-impact assessment report, or available SDK. Financial information is represented only by years rather than performance metrics, so credibility cannot be judged. Customer references are stated, but Fortune 500 collaboration is...
Supplier typeThe supplier is presented as a manufacturing and turnkey project provider for machinery, including ALU cutters, drilling, engraving, lathe, and panel-cutting equipment. It operates three production lines, serves broad international markets, and describes itself as a turnkey solution provider.
CertificationsThe supplier reports ISO9001:2015 certification, with ASME, ISO 9001, and GMP also listed among its management-system certifications. This is explicit evidence of multiple relevant certifications, although the slices do not provide certificate scope or validity details for each item.
After-Sales capabilityThe supplier has in-stock service capacity, overseas agents or branches, and trade-show participation, but it has no written procedures or records for corrective/preventive actions or customer complaint handling. Finished-product inspection instructions exist without written records, indicating a documented-service weakness.
Production capacityThe supplier reports three production lines, in-stock service capability, a broad machinery facility, and 2–3 month lead times in both peak and off-peak seasons. Nevertheless, it lacks a valid contract governing manufacturing capacity with its related subcontractor, which is a stated capacity-management deficiency.
Customization capabilityCustomization is explicitly available from samples, customer designs, and through full customization. The supplier also reports R&D personnel, CAD and PORTAL tools, and documented design-development controls, providing direct support for customization capability.

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