What payment terms are accepted?

Accepted payment terms include LC, T/T, D/P, PayPal, Western Union, and small-amount payments.

Does the project include regulatory compliance support?

Yes, the turnkey project ensures compliance with FDA and EMA guidelines and provides documentation assistance.

What is the production capacity of the granulator?

The production capacity ranges from 15/30 to 300/500 kg per batch.

GMP Approved Ready-to-Use Fully-Integrated Pharmaceutical & Medical Project/ Pharmaceutical Equipment

Name: GMP Approved Ready-to-Use Fully-Integrated Pharmaceutical & Medical Project/ Pharmaceutical Equipment
Brand: Shanghai Iven Pharmatech Engineering Co., Ltd.
SKU: 2085011305

Shanghai, ChinaShanghai Iven Pharmatech Engineering Co., Ltd.

US$200,000.00-600,000.00

1 Piece

Product profile

Certification

CE, GMP, ISO, GMP

Customized

Production Capacity (Kg/Batch)

15/30--300/500

Model NO.

customized

Dimension(LWH)

1.5*1.3*5m--3.5*3.5*10m

Vessel Volume(L)

45-1530

Fan Power(Kw)

7.5-75

Electric Heating Power(Kw)

30-120

Steam Consumption(Kg/H)

180-677

Weight of Mian Machine(Kg)

800-3500

Finished Dosage Form

Granules

Precision

High Precision

Voltage

380V

Computerized

Condition

New

Warranty

Field Installation, Commissioning and Training

After-sales Service

Field Installation, Commissioning and Training

Transport Package

Standard Export Package

Specification

3.2 x2.5 x2.5M

Trademark

IVEN

Origin

China

Production Capacity

Customized

Key features

GMP & CE Certified: Fully compliant with GMP, CE, and ISO standards for pharmaceutical manufacturing.

Turnkey Project Solution: Complete facility design, equipment procurement, installation, and training for immediate operation.

Full Customization Options: Offers full customization, minor customization, and flexible customization based on samples or designs.

High Precision Manufacturing: Equipped with PLC, engine, and motor for high precision production of granules and oral solid dosage forms.

Comprehensive After-Sales Service: Includes field installation, commissioning, training, online support, and maintenance services.

Flexible Production Capacity: Adjustable capacity from 15/30 to 300/500 kg/batch to suit various production needs.

1-Year Core Component Warranty: Provides a 1-year warranty on core components including PLC, engine, and pressure vessel.

Global Regulatory Compliance: Designed to meet FDA and EMA guidelines ensuring smooth regulatory approval and market entry.

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: ≤1.57h 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.