What is the lead time for delivery?

Lead time is 1 to 3 months, depending on the season.

What payment terms are accepted?

We accept LC, T/T, D/P, PayPal, Western Union, and small-amount payments.

Does the service include installation and training?

Yes, we provide field installation, commissioning, and training for skilled workers.

Lvp Integrated Turnkey Project

Name: One-Stop Pharmaceutical Industry IV Solution Turnkey Project / IV Fluids/ Normal Saline/ Ivf/ Lvp Integrated Turnkey Project
Brand: Shanghai Iven Pharmatech Engineering Co., Ltd.
SKU: 2064393005

Shanghai, ChinaShanghai Iven Pharmatech Engineering Co., Ltd.

US$300,000.00-1,200,000.00

1 Piece

Product profile

Application

Pharmaceutical Industry

Disposable

Warranty

1 Year

Capacity

100ml, 250ml, 500ml.1000ml

Weight

3-12t

Power

32kw

Function

Filling Equipment

Key Selling Points

Automatic

Weight (Kg)

3500 Kg

Applicable Industries

Manufacturing Plant, Pharma

Product Capacity

5800~6500 Bags/ Hour

Bag-Making Film

Non-PVC Film

Bag-Making Form

Single Port, Heat Insulation Seal

Overall Size

3.26X2.0 X2.1m--8.97X4.65 X2.25m

Packaging

Wooden Case

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

Cartons; Wooden Case;

Specification

3.2 x2.5 x2.5M

Trademark

IVEN

Origin

China

Production Capacity

2 PCS/Year

Key features

100% Film Utilization: No waste edges between bags, saving material and energy consumption significantly.

Quick Size Changeover: Switch from one IV bag size to another in just 0.5 to 1 hour.

High Precision Filling: Patent contact filling nozzle prevents overflow and particle generation.

Low Leakage Rate: Reliable heating and welding system ensures leakage rate below 0.03%.

Compact Machine Design: Reduced length by 1/3, saving room space and running costs.

Full Turnkey Solution: Includes clean room, water treatment, filling, packing, and quality control systems.

GMP Compliant: Complies with EU GMP, US FDA cGMP, PICS, and WHO GMP standards.

Customizable Capacity: Available in 100ml, 250ml, 500ml, and 1000ml with flexible customization options.

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.