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Cell Therapy Turnkey Project
US$250,000.00-800,000.00
1 Piece

Product profile

Warranty

1 Year

Finished Dosage Form

Liquid

Precision

High Precision

Certification

CE, GMP, ISO

Voltage

380V

Computerized

Computerized

Customized

Customized

Condition

New

After-sales Service

Field Installation, Commissioning and Training

Transport Package

Wooden Case

Specification

9620.00cm * 2540.00cm * 2330.00cm

Trademark

IVEN

Origin

China

Production Capacity

Customized

Key features

Turnkey Factory Setup: Complete cell therapy factory setup with advanced technology and international process control.
GMP & FDA Documentation: Full documentation support including IQ/OQ/PQ/DQ/FAT/SAT to help obtain GMP & FDA certificates.
Global Project Experience: Successfully built 20+ pharmaceutical and medical turnkey plants in Russia, Uzbekistan, Indonesia, etc.
Professional Technical Team: Expert team providing onsite training and long-term technical assurance for injectable vial plants.
Flexible Customization: Offers customization from samples, designs, full customization, minor customization, and flexible options.
High Precision Manufacturing: Produces high precision liquid dosage forms with CE, GMP, and ISO certifications.
Risk Avoidance Strategy: Professional experience helps finish plants in shortest time while avoiding potential risks.
100% Product Inspection: Strict 100% visual and function inspection for finished products with traceable raw materials.

Company profile

Shanghai Iven Pharmatech Engineering Co., Ltd.
Years of Export ExperienceLow MOQPatents AwardedProduct Certification
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: ≤1.54h 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 does the turnkey plant include?
A:
The IVEN Injectable oncology vial turnkey plant includes advanced technology support, international qualified process control, and full documentation for GMP & FDA certification.
Q:What certifications are available?
A:
The equipment comes with CE, GMP, and ISO certifications. Full documentation (IQ/OQ/PQ/DQ/FAT/SAT) is provided to help obtain GMP & FDA certificates.
Q:What is the warranty period?
A:
The product comes with a 1-year warranty.
Q:What after-sales services are provided?
A:
Services include field installation, commissioning, and training. The professional technical team provides long-term technical assurance.
Q:What is the minimum order quantity?
A:
The Minimum Order Quantity (MOQ) is 1 Set.

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