What is the expected lifetime of the cleanroom system?

The estimated lifetime is between 5 to 10 years.

How is quality control handled for finished products?

We perform 100% inspection, including both visual and functional checks, following uniform instructions.

Sanitized Workspace Development Antiseptic Testing Dust-Free Pharmaceutical Research Aseptic for Drug Manufacturing Cleanroom with CE

Name: Sanitized Workspace Development Antiseptic Testing Dust-Free Pharmaceutical Research Aseptic for Drug Manufacturing Cleanroom with CE
Brand: Shanghai Iven Pharmatech Engineering Co., Ltd.
SKU: 2067133455

Shanghai, ChinaShanghai Iven Pharmatech Engineering Co., Ltd.

US$10,000.00-80,000.00

1 Piece

Product profile

Certification

CE, ISO9001

Application

Hotel, Pharmaceutical

Usage

HAVC System

Model NO.

Customized IVEN -2

Standard Export Package

Standard/Customized

Model Number

HVAC System for Clean Room

Color

Customized Color

Design Style

Industrial

Lifetime

5~10 Years

Mounting

Ceiling Mount

Transport Package

Standard Export Package

Specification

customized

Trademark

IVEN

Origin

China

Production Capacity

Customized

Key features

Customized Color Options: Color is explicitly listed as Customized Color in the product attributes.

CE and ISO9001 Certified: Product holds CE and ISO9001 certifications for quality and safety compliance.

Comprehensive HVAC Solution: Includes HEPA filtration, air shower, interlocks, and full ventilation system installation.

Pharmaceutical Grade Control: Maintains strict temperature, humidity, and pressure for contamination control.

Energy Cost Savings: Efficient heating and cooling tailored to facility needs reduces operational costs.

100% Finished Product Inspection: Every unit undergoes visual and functional inspection before shipment.

Flexible Customization: Supports customization from samples, designs, and full or minor modifications.

19 Years Export Experience: Manufacturer with 19 years of export history and established global supply chain.

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: ≤2.19h 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.