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Modular Clean Room System Turnkey Project
US$1,000.00-20,000.00
1 Piece
Product profile
Customization
AvailableCertification
GS, RoHS, CE, ISO9001, GMPNoise
70-90dbModel NO.
HM MCRApplication
IndustrialControl Mode
Remote ControlUsage
Dust Removal, Smoke Removal, Adding Negative Ion, HumidificationAfter Service
1 YearStaff Training
as RequiredTransport Package
Sea Worthy PackingSpecification
as requiredTrademark
HM PHARMACHINEOrigin
Zhejiang ChinaHS Code
8422303001Production Capacity
30 Per YearKey features
Turnkey Project Solution: Complete service from facility engineering design, manufacturing, supply to construction, installation, commissioning, and validation.
European Technology & Quality: Combines European technology with Chinese manufacturing for high cost-effective, reliable solutions meeting European standard quality.
Comprehensive Certifications: Holds ISO 9001, GS, RoHS, CE, and GMP certifications, complying with WHO, EU, FDA, TGA, and MHRA regulations.
Wide Industry Application: Suitable for pharmaceutical, biotech, medical, healthcare, food, cosmetics, electronic, and solar industries.
Advanced HPL Modular System: Features high-class HPL modular panels with advanced flushed doors and windows for clean room environments.
Experienced Engineering Team: Backed by 50 experienced engineers and European experts ensuring technical support and quality control.
Multi-functional Usage: Provides dust removal, smoke removal, negative ion addition, and humidification capabilities.
International Compliance: Meets ISO14644 and US FED STD 209E standards, ensuring global regulatory compliance for clean room projects.
Company profile
Business Type: Manufacturer/FactoryExport Year: 1999-03-18Nearest Port: SHANGHAI,CHINA, NINGBO ,CHINAAverage Response Time: ≤0.96hTerms 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 is the warranty period for the clean room system?
A:
The after-service warranty period is 1 year.
Q:What certifications does the HM Modular Clean Room System hold?
A:
The system holds GS, RoHS, CE, ISO9001, and GMP certifications, complying with WHO, EU, FDA, TGA, and MHRA regulations.
Q:What industries can this clean room system be applied to?
A:
It is suitable for pharmaceutical, laboratory, biotech, medical, hospital, healthcare, food, cosmetics, electronic, and solar industries.
Q:What is the average lead time for delivery?
A:
The average lead time is 1-3 months for both peak and off-season periods.
Q:What payment terms are accepted?
A:
Accepted payment terms include LC, T/T, D/P, Western Union, and Money Gram.
Send Inquiry
*To:
HM Pharmaceutical Engineering & Project (Zhejiang) Co., Ltd.
HM Pharmaceutical Engineering & Project (Zhejiang) Co., Ltd.*Content:
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