What certifications does the machine have?

The machine holds CE, GMP, and ISO certifications.

How long is the lead time for production?

The average lead time is one month during peak season and 1-3 months during off-season.

Pharmaceutical & Medical & Chemcial Granulating Machine Used in Powder and Granule

Name: Pharmaceutical & Medical & Chemcial Granulating Machine Used in Powder and Granule
Brand: Shanghai Iven Pharmatech Engineering Co., Ltd.
SKU: 2056439795

Shanghai, ChinaShanghai Iven Pharmatech Engineering Co., Ltd.

US$50,000.00-250,000.00

1 Piece

Product profile

Certification

CE, GMP, ISO

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

Type

Preparation Machinery

Finished Dosage Form

Granules

Precision

High Precision

Voltage

380V

Computerized

Customized

Condition

New

Warranty

1 Year

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

Continuous Granulation Process: Integrates extrusion, crushing, and granulating to directly convert powder into granules.

GMP Compliant Design: Closed working state with easy cleaning to prevent dust leakage and cross-contamination.

No Drying Required: Dry granulation eliminates water addition and drying, preserving active ingredients.

Modular Construction: Compact structure with separated power and work sections for better space utilization.

Water-Cooled Rollers: Equipped with water-cooled pressure rollers for stable operation in hot environments.

Wide Customization Options: Available in full, minor, and flexible customization based on samples or designs.

High Precision Output: Two-stage sizing system ensures granules meet desired size specifications accurately.

1-Year Warranty Coverage: Includes field installation, commissioning, and training support for one year.

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: ≤2.16h 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.