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High Reliable Cleanroom System / Portable Pharmaceutical GMP Modular Dust Free Clean Room Equipment
US$10,000.00-80,000.00
1 Piece
Product profile
Certification
CE, ISO9001Application
Hotel, PharmaceuticalUsage
HAVC SystemModel NO.
Customized IVEN -2Standard Export Package
Standard/CustomizedModel Number
HVAC System for Clean RoomColor
Customized ColorDesign Style
IndustrialLifetime
5~10 YearsMounting
Ceiling MountTransport Package
Standard Export PackageSpecification
customizedTrademark
IVENOrigin
ChinaProduction Capacity
CustomizedKey features
Customized Color Options: Color is customizable to meet specific project requirements.
Comprehensive Certification: Certified with CE and ISO9001 standards for quality assurance.
Pharmaceutical Grade HVAC: Specialized HVAC system for controlled temperature and humidity.
Contamination Control: Maintains cleanroom environment free from airborne pollutants.
Full Turnkey Solution: Includes design, construction, HVAC installation, and validation.
Durable Construction: Uses steel sandwich panels and epoxy/PVC flooring for longevity.
Energy Efficient: Tailored heating and cooling to reduce operational energy costs.
Regulatory Compliance: Designed to meet strict pharmaceutical industry safety standards.
Company profile
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: ≤1.46h 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.
Product Q&A
Q:What certifications does the cleanroom system have?
A:
The system is certified with CE and ISO9001 standards.
Q:Is the color of the cleanroom customizable?
A:
Yes, the color is customizable to suit your specific needs.
Q:What is the minimum order quantity?
A:
The minimum order quantity is 1 set.
Q:What is the average lead time for production?
A:
The average lead time is 1-3 months, depending on the season.
Q:What payment terms are accepted?
A:
We accept LC, T/T, D/P, PayPal, Western Union, and Small-amount payment.
Send Inquiry
*To:
Shanghai Iven Pharmatech Engineering Co., Ltd.
Shanghai Iven Pharmatech Engineering Co., Ltd.*Content:
Supplier replies will be sent to your registered email
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