What is the minimum order quantity?

The minimum order quantity is 1 set.

What are the payment terms?

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

What is the lead time for production?

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

Ready-to-Use Comprehensive Pharmaceutical Project / Pharmaceutical Equipment with GMP

Name: Ready-to-Use Comprehensive Pharmaceutical Project / Pharmaceutical Equipment with GMP
Brand: Shanghai Iven Pharmatech Engineering Co., Ltd.
SKU: 2085009025

Shanghai, ChinaShanghai Iven Pharmatech Engineering Co., Ltd.

US$200,000.00-300,000.00

1 Piece

Product profile

Application

Clinical Diagnosis, Pharmaceutical Industry

Disposable

Injection Site

Intravenous

Model NO.

customized

Material

Rubber, Silicone, Stainless Steel

Safety Feature

Auto-Retractable Needle, Needle Guard

Usage

Medical, Vaccine Administration

Warranty

Field Installation, Commissioning and Training

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

Certification

CE, GMP, ISO

Voltage

380V

Computerized

Customized

Condition

New

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, procurement, installation, and training for oral solid dosage production.

GMP & Regulatory Compliance: Facilities designed to meet FDA/EMA standards with CE, GMP, and ISO certifications.

High Precision Granulator: Advanced fluid bed granulator with PLC control and high-precision output capabilities.

Flexible Customization: Customizable production capacity, dimensions, and power to match specific manufacturing needs.

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

Time & Cost Efficiency: Streamlined project management reduces setup time and lowers overall equipment costs.

Quality Control Support: Includes validation support, documentation assistance, and standardized QC procedures.

Proven Manufacturer: Established in 2005 with 19 years of export experience and 57 skilled employees.

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: ≤1.46h 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 is included in the turnkey project?

The turnkey project includes conceptual design, detailed engineering, procurement, installation, commissioning, validation, training, and handover of the complete facility.

Q:What certifications does the equipment have?

The equipment holds CE, GMP, and ISO certifications, ensuring compliance with international pharmaceutical standards.

Q:Can the machine specifications be customized?

Yes, customization options include production capacity, dimensions, vessel volume, power, and other parameters to fit specific needs.

Q:What is the warranty period for core components?

The warranty for core components is 1 year, covering parts and labor for mechanical defects.

Q:What after-sales services are provided?

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