Does the machine require water or liquid for operation?

No, the dry granulation process does not add water or other liquids, eliminating the need for drying.

What certifications does the product hold?

The product is certified with CE, GMP, and ISO standards.

Easy-to-Use Pharmaceutical Dry Powder Compaction Press Machine/ Powder Briquetting Equipment

Name: Easy-to-Use Pharmaceutical Dry Powder Compaction Press Machine/ Powder Briquetting Equipment
Brand: Shanghai Iven Pharmatech Engineering Co., Ltd.
SKU: 2060165445

Shanghai, ChinaShanghai Iven Pharmatech Engineering Co., Ltd.

US$50,000.00-250,000.00

1 Piece

Product profile

After-sales Service

Field Installation, Commissioning and Training

Certification

CE, GMP, ISO

Condition

New

Customized

Voltage

380V

Type

Preparation Machinery

Finished Dosage Form

Granules

Precision

High Precision

Computerized

Warranty

1 Year

Transport Package

Standard Export Package

Specification

3.2 x2.5 x2.5M

Trademark

IVEN

Origin

China

Production Capacity

Customized

Key features

Multi-Function Integration: Combines compaction, crushing, and grinding into a single unit for streamlined processing.

No Drying Required: Eliminates water or liquid addition, preventing active ingredient loss through decomposition.

GMP Compliant Design: Meets pharmaceutical GMP requirements with separated power and work sections to prevent cross-contamination.

Enhanced Product Uniformity: Produces granules with consistent particle size and shape for improved final product quality.

Cost-Effective Process: Requires less equipment, energy, and time compared to traditional wet granulation methods.

Reduced Dust Emission: Dry granulation process generates less dust, enhancing safety and preventing environmental contamination.

Modular & Compact Structure: Features an overall modular design with better space utilization and easy maintenance.

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

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: ≤2.21h 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.