What after-sales services are provided?

We provide online support, field installation, commissioning, training, and maintenance services globally.

What are the lead times for production?

Lead time is typically one month during the off-season and 1-3 months during the peak season.

Is the system computerized and automated?

Yes, it features a computerized control system with intelligent PID control, automatic sterilization, and data recording functions.

Hybridoma Technology Apparatus/Perfusion Bioreactor System in China

Name: Hybridoma Technology Apparatus/Perfusion Bioreactor System in China
Brand: Shanghai Iven Pharmatech Engineering Co., Ltd.
SKU: 2071388965

Shanghai, ChinaShanghai Iven Pharmatech Engineering Co., Ltd.

US$50,000.00-500,000.00

1 Piece

Product profile

Material

Wet Part Is SS316L(Alltank Body)and Other Is SS304

Warranty

1 Year

Working Pressure Inside Vessel

0.25MPa

Model NO.

Customized IVEN -11

Working Pressure Inside Jacket

0.3MPa

PLC

Self-Developing PLC/Siemens PLC

Basic Functions

Culture Microorganism, Adjust pH, Do, Temp.Antifoa

Optional Functions

Weigh, Pressflow, Discharged Gas Detect, Multi-Fee

Capacity

50L-500L

Type

Preparation Machinery

Finished Dosage Form

Liquid

Precision

High Precision

Certification

CE, GMP, ISO

Voltage

380V

Computerized

Customized

Condition

New

After-sales Service

Field Installation, Commissioning and Training

Transport Package

Wooden Case

Specification

customized

Trademark

IVEN

Origin

China

Production Capacity

Customized

Key features

GMP Compliant Design: Manufactured strictly following GMP standards with S88 and GAMP5 compliant control systems.

High Precision Control: Features intelligent PID pH control, automatic sterilization, and precise temperature management.

Versatile Culture Support: Suitable for full-suspension, carrier, and microcarrier cultures for antibodies and vaccines.

Durable Construction: Wet parts use SS316L and other parts SS304 stainless steel for anti-corrosive performance.

Flexible Customization: Offers full customization from samples/designs with capacities ranging from 50L to 500L.

Comprehensive After-Sales: Provides field installation, commissioning, training, and online support for global clients.

Advanced Automation: Equipped with self-developed or Siemens PLC, audit trails, and electronic signature functions.

Proven Manufacturer: Established in 2005 with 19 years of export experience and ISO/CE certifications.

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: ≤1.47h 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.