What preparations are needed for setting up an IV plant?

You need to prepare the land, building construction, water supply, and electricity.

What certifications does the equipment have?

The equipment holds ISO and CE certifications.

Can you arrange a visit to your user projects?

Yes, we invite clients to visit our turnkey projects in countries like Indonesia, Vietnam, Uzbekistan, and Tanzania.

Ampoule Decontamination, Liquid Dispensing, and Capping Line/Integrated Ampoule Packaging System: Wash, Fill, Seal

Name: Ampoule Decontamination, Liquid Dispensing, and Capping Line/Integrated Ampoule Packaging System: Wash, Fill, Seal
Brand: Shanghai Iven Pharmatech Engineering Co., Ltd.
SKU: 1931389221

Shanghai, ChinaShanghai Iven Pharmatech Engineering Co., Ltd.

US$40,000.00-150,000.00

1 Piece

Product profile

Warranty

Field Installation, Commissioning and Training

Filling Capacity

100-600bpm

Process Type

Washing, Sterilizing, Filling, Stoppering, Capping

Model NO.

Customized IVEN -1

Capacity

Standard/Customized;

Optional Configuration

Inspection, Labeling, Blistering, Cartoning

Applicable Bottle

1-30ml Glass Vial Bottle

Filling Pumps

Glass Pump, Metal Pump, Peristaltic Pump, Ceramic

Packing Material

PVC/PE or Pet/PE

Suitable Ampoule Volume

2-25ml/Ampoule

Name

Plastic / Glass Ampoule Filling Sealing Machine

Product Specification

Meet with GMP Standards

Filling Liquid

Pharmaceutical, Cosmetic, Oral, Oil, Pesticide

Filling Valve Head

Multi-Head

Automatic Grade

Fully Automatic

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

Wooden Package

Specification

2500*2500*1300 mm - 4280*1650*2400 mm

Trademark

IVEN

Origin

China

HS Code

8422303090

Production Capacity

7000~10000 PCS/H

Key features

GMP Standard Compliance: Meets GMP production standards with closed cleaning operations to prevent contamination.

High Automation Stability: Features lower fault rates, compact design, and stable continuous operation from washing to sealing.

Advanced Ultrasonic Washing: Utilizes water and compressed air cross-pressure jet wash combined with ultrasonic cleaning for superior results.

Universal Ampoule Compatibility: Suitable for 1-20ml ampoules and can be adapted for vial washing, filling, and capping lines.

Precision Filling Technology: Employs multi-needle filling with ceramic injection pumps ensuring high precision and low error tolerance.

Customizable Configuration: Offers optional configurations including inspection, labeling, blistering, and cartoning modules.

Low Maintenance Design: Features wear-proof manipulators and hinge-type seat heat structures for convenient maintenance.

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: ≤2.46h 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:Can the machine be customized according to our requirements?

Yes, we offer full customization including customization from samples, designs, and flexible minor adjustments.

Q:Does the equipment meet GMP, FDA, and WHO standards?

Yes, we design and manufacture the equipment in accordance with GMP, FDA, and WHO requirements specific to your country.

Q:What are the payment terms?

Generally, we accept TT or irrevocable L/C at sight.

Q:What is the after-sales service policy?

We reply within 24 hours via email or phone. If a local agent is available, they will visit your site within 24 hours. We also provide engineer dispatch for 6-12 months.

Q:How long does a turnkey project take?

It takes about 1 year from designing the layout to finishing installation and commissioning.