What certifications does the equipment hold?

The product is certified with CE, GMP, and ISO standards, ensuring compliance with international safety and quality regulations.

What is the minimum order quantity?

The minimum order quantity is 1 set, making it suitable for both pilot trials and industrial production needs.

What after-sales services are provided?

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

Versatile Biopharma Bioreactors: 50L to 500L Capacity Solutions

Name: Versatile Biopharma Bioreactors: 50L to 500L Capacity Solutions
Brand: Shanghai Iven Pharmatech Engineering Co., Ltd.
SKU: 2166451325

Shanghai, ChinaShanghai Iven Pharmatech Engineering Co., Ltd.

US$50,000.00-500,000.00

1 Piece

Product profile

Application

Clinical Diagnosis, Pharmaceutical Industry

Disposable

Injection Site

Intravenous

Model NO.

Customized IVEN -11

Material

Glass, Stainless Steel, Wet Part Is SS316L(Alltank Body)and Other Is SS304

Safety Feature

Auto-Retractable Needle, Locking Mechanism, Needle Guard, Tamper-Evident Seal

Usage

Medical

Warranty

1 Year

Working Pressure Inside Vessel

0.25MPa

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 & ASME-BPE Compliance: Design and manufacture strictly follow GMP regulations and ASME-BPE requirements for pharmaceutical safety.

One-Button Sterilization: Features fully automatic sterilization with a single button operation for efficiency and safety.

Flexible Control Systems: Supports single tank control or multi-tank joint control with independent management capabilities.

Comprehensive Alarm Functions: Automatically alarms when parameters exceed set upper or lower limits to ensure process safety.

CIP and SIP Capabilities: Equipped with jacket systems for Cleaning In Place (CIP) and Sterilization In Place (SIP).

Audit Trail Function: Includes audit trail features to fully meet GMP data integrity and traceability requirements.

Customized Engineering Solutions: Offers full customization from samples and designs to meet specific national pressure vessel standards.

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: ≤2.17h 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.