What is the minimum order quantity?

The minimum order quantity is 1 set.

What is the average lead time for delivery?

The average lead time is 1 to 3 months, depending on the season.

Does the system include after-sales service?

Yes, after-sales service includes field installation, commissioning, and training for skilled workers.

Innovative Non-Toxic Soft Bag IV Solution Turnkey Project for Pharmaceutical Industry

Name: Innovative Non-Toxic Soft Bag IV Solution Turnkey Project for Pharmaceutical Industry
Brand: Shanghai Iven Pharmatech Engineering Co., Ltd.
SKU: 2062215435

Shanghai, ChinaShanghai Iven Pharmatech Engineering Co., Ltd.

US$190,000.00-500,000.00

1 Piece

Product profile

Application

Clinical Diagnosis, Forensic Science, Pharmaceutical Industry, Pharmaceutical & Chemical

Disposable

Material

Plastic, Stainless Steel

Model NO.

customized

Safety Feature

Locking Mechanism, Needle Guard, Tamper-Evident Seal, as Requested

Usage

Medical, Vaccine Administration, Pharmaceutical & Medical

Warranty

1 Year

Video Outgoing-Inspection

Provided

Bag-Making Film

Non-PVC Film

Bag-Making Form

Single Port, Heat Insulation Sealing

Power

32kw

Weight

3-12t

Key Selling Points

Automatic;Accuracy; High Speed;

Applicable Industries

Pharmaceutical

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: Special 130mm width design ensures no waste edge between bags, saving material and energy.

Quick Size Changeover: Switch between IV bag sizes in just 0.5-1 hour, enhancing production flexibility.

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

Compact Machine Structure: Reduces machine length by 1/3, saving room space and lowering running costs.

Low Leakage Rate: Reliable heating and welding system ensures IV bag leakage rate is less than 0.03%.

Automatic Quality Control: Auto detection and faulty rejection system automatically rejects unqualified IV bags.

GMP Compliant Design: Integrated engineering solutions comply with EU GMP, US FDA cGMP, PICS, and WHO GMP.

Customized Engineering: Full customization available from samples, designs, or minor adjustments to fit specific needs.

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: ≤1.61h 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.