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Advanced Process Engineering for Fermentation/Cutting-Edge Fermentation Technology
US$50,000.00-500,000.00
1 Piece

Product profile

Warranty

1 Year

Finished Dosage Form

Liquid

Precision

High Precision

Model NO.

Customized IVEN -11

Certification

CE, GMP, ISO

Voltage

380V

Computerized

Computerized

Customized

Customized

Condition

Field Installation, Commissioning and Training

Transport Package

Wooden Case

Trademark

IVEN

Origin

China

Production Capacity

Customized

Key features

Customized Solutions: Provides customized integrated engineering solutions tailored to user needs in the biopharmaceutical industry.
High Precision Control: Features high precision with Siemens PLC and MP277 HMI for reliable automatic control of production and cleaning.
3D Modular Design: Adopts a 3D modular design that is compact, beautiful, and generous, ensuring efficient space utilization.
Premium Components: Main materials like tanks, pumps, and valves are selected from international and domestic excellent brands.
GMP5 Compliance: Design and inspection conform to GAMP5 V-model, providing complete verification files (RA, DQ, IQ, OQ).
Versatile Application: Suitable for recombinant protein drugs, antibody drugs, vaccines, and blood products production.
CE Certified: Product holds CE certification, ensuring compliance with European safety and quality standards.
1 Year Warranty: Comes with a 1-year warranty covering the equipment for peace of mind and quality assurance.

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: ≤1.46h 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 industries does this bioreactor serve?
A:
It serves the biopharmaceutical industry, including recombinant protein drugs, antibody drugs, vaccines, and blood products.
Q:Is customization available for this system?
A:
Yes, we provide customized integrated engineering solutions, including minor, flexible, and full customization from samples or designs.
Q:What control system is used in the bioreactor?
A:
The system uses Siemens 300 series PLC and MP277 series touch screen HMI, conforming to GAMP5 V-model standards.
Q:What certifications does the product have?
A:
The product is certified with CE, GMP, and ISO standards to ensure quality and safety.
Q:What is the warranty period?
A:
The product comes with a 1-year warranty.

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