How long is the lead time?

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

What after-sales services are provided?

We provide online support, field maintenance, repair services, and comprehensive training for your personnel.

Where is the machine manufactured?

The machine is manufactured in Shanghai, China, by a company with 19 years of export experience.

Pharmaceutical Machine with GMP

Name: End-to-End Total Package Pharmaceutical Turnkey Project/Comprehensive& Holistic Project /Pharmaceutical Machine with GMP
Brand: Shanghai Iven Pharmatech Engineering Co., Ltd.
SKU: 2079779355

Shanghai, ChinaShanghai Iven Pharmatech Engineering Co., Ltd.

US$200,000.00-600,000.00

1 Piece

Product profile

Application

Chemical Industry, Clinical Diagnosis, Cosmetic Industry, Pharmaceutical Industry, Healthcare Industry

Certification

CE, GMP, ISO

Control System

Automation

Model NO.

customized

Customized

Production Capacity (Kg/Batch)

15/30--300/500

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

Turnkey Project Solution: Complete facility design, equipment procurement, installation, and training for oral solid dosage production.

GMP & Regulatory Compliance: Facility and processes designed to meet FDA, EMA, and GMP standards with validation support.

High Precision Granulator: Advanced fluid bed granulator with high precision, PLC control, and core components warranty.

Customizable Specifications: Flexible customization options for production capacity, dimensions, and power based on client needs.

Cost and Time Efficiency: Streamlined project management reduces setup time and costs associated with individual sourcing.

Comprehensive After-Sales: Includes field installation, commissioning, training, and online support for long-term reliability.

Wide Application Range: Suitable for pharmaceutical, chemical, cosmetic, and healthcare industries for various dosage forms.

Expert Engineering Team: Leverages 19 years of experience with 5 R&D engineers for optimized process and risk management.

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: ≤1.43h 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.