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Hm Modular Cleanroom Design and Manufacturing
US$5,000.00-200,000.00
1 Piece

Product profile

Customization

Available

Certification

GS, RoHS, CE, ISO9001, GMP

Noise

40-60db

Model NO.

HM PCR

Application

Industrial

Control Mode

Remote Control

Usage

Dust Removal, Smoke Removal, Adding Negative Ion, Humidification, Sterilization

OEM

Suitable

Clean Level

100-10000

Fire Resistance

Class a,B,C,D,E

Transport Package

Seaworthy Packing

Specification

as required

Trademark

HM PHARMACHINE

Origin

Zhejiang China

Production Capacity

1000

Key features

Multi-System Integration: Complete solutions including partitions, HVAC, lighting, flooring, and monitoring systems.
Global Compliance: Certified with ISO 9001, EU CE, WHO GMP, US FDA, and other international standards.
Customizable Clean Levels: Supports clean room levels from Class 100 to Class 10000 based on project needs.
European Quality Standard: Combines European technology with Chinese manufacturing for high cost-effectiveness.
Versatile Applications: Suitable for pharmaceutical, biotech, healthcare, and industrial dust/smoke removal.
Expert Engineering Team: 50 experienced engineers guided by European experts for design and manufacturing.

Company profile

HM Pharmaceutical Engineering & Project (Zhejiang) Co., Ltd.
Importers and ExportersYears of Export ExperienceMulti-language PioneerSelf-branded
Business Type: Manufacturer/FactoryExport Year: 1999-03-18Nearest Port: SHANGHAI,CHINA, NINGBO ,CHINAAverage Response Time: ≤3.06hTerms 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.

Product Q&A

Q:What certifications does the cleanroom system have?
A:
The system is certified with ISO 9001, GS, RoHS, CE, and GMP, complying with WHO GMP, US FDA, and EU cGMP standards.
Q:What are the available clean room levels?
A:
We offer customizable clean room levels ranging from Class 100 to Class 10000.
Q:What is the average lead time for production?
A:
The average lead time is 1-3 months for both peak and off-peak seasons.
Q:What payment terms are accepted?
A:
We accept LC, T/T, D/P, Western Union, and Money Gram.
Q:Which industries can use this modular cleanroom?
A:
It is mainly used for pharmaceutical, life sciences, biotech, healthcare, and industrial applications.

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