What is the lead time for production?

The average lead time is one month, ranging from 1 to 3 months depending on the season and order specifics.

What is the control system type?

The machine features a PLC control system that automatically completes operations and prints reliable process records.

High Shear Granulation and Drying Process Equipment with Advanced Control Systems for Precise and Reliable Performance

Name: High Shear Granulation and Drying Process Equipment with Advanced Control Systems for Precise and Reliable Performance
Brand: Shanghai Iven Pharmatech Engineering Co., Ltd.
SKU: 2052382535

Shanghai, ChinaShanghai Iven Pharmatech Engineering Co., Ltd.

US$25,000.00-250,000.00

1 Piece

Product profile

Certification

CE, GMP, ISO

Applicable Industry

Food, Pharmaceutical, Cosmetic, Chemicals

Cutting Speed

0-2900r/Min

Compressed Air

0.4-0.6MPa

Applicable Materials

Wet or Dry

Mixing Efficiency

99.9%

Finished Dosage Form

Granules

Precision

High Precision

Voltage

220V

Computerized

Customized

Condition

New

Warranty

1 Year

After-sales Service

Life Term Technical Support

Transport Package

Wooden Case

Specification

Stainless steel

Trademark

IVEN

Origin

China

Production Capacity

Customized

Key features

Advanced PLC Control: Automatically completes operations based on user settings and prints reliable original records of all process parameters.

Wide Application Scope: Suitable for pharmaceutical, food, chemical, and cosmetic industries for wet or dry material granulation and mixing.

Flexible Customization: Offers full customization, minor customization, and flexible options based on samples or designs.

Life Term Support: Provides life term technical support to ensure long-term equipment reliability and operational continuity.

High Precision Performance: Delivers high precision granulation with mixing efficiency up to 99.9% and precise control over process parameters.

Multiple Capacity Options: Available in 8 models ranging from 100L to 800L nominal volume, with batch capacities from 20kg to 320kg.

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: ≤1.43h 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.