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Comprehensive Turnkey Solid Dosage Setup/Pharmaceutical & Medical Fully-Integrated Project/End-to-End Turnkey Project
US$200,000.00-800,000.00
1 Piece

Product profile

Certification

CE, GMP, ISO

Warranty

Field Installation, Commissioning and Training

Application

Pharmaceutical Food Industries;Medical;

Model NO.

customized

Video Outgoing-Inspection

Provided

Core Components

Motor, Engine

Feature

High Efficiency Tablet Press Machine

After Warranty Service

Video Technical Support on

Function

Automatic Powder Suction Press Tablet

Key Selling Points

High-Accuracy

Finished Dosage Form

Tablet

Precision

High Precision

Voltage

380V

Computerized

Computerized

Customized

Customized

Condition

New

After-sales Service

Field Installation, Commissioning and Training

Transport Package

Wooden Package

Specification

12000*950*1850mm

Trademark

IVEN

Origin

China

HS Code

8474802000

Production Capacity

Customized

Key features

Turnkey Project Solution: Complete facility design, engineering, installation, and training for oral solid dosage production.
High Precision Tablet Press: Advanced automatic powder suction technology with high-accuracy tablet compression capabilities.
Full Customization Options: Flexible customization from samples, designs, minor adjustments to full project customization.
Comprehensive Training Support: On-site training for personnel on operation, maintenance, hygiene, and safety standards.
Regulatory Compliance: Facilities designed to meet FDA, EMA, GMP, and CE standards for global market access.
High Efficiency Production: Capable of producing up to 260,000 tablets per hour with stable and consistent output.
Integrated Engineering Services: Includes clean rooms, water treatment, HVAC, and quality control systems for end-to-end setup.
Video Inspection Available: Video outgoing inspection provided to verify equipment quality before shipment.

Company profile

Shanghai Iven Pharmatech Engineering Co., Ltd.
Years of Export ExperienceLow MOQPatents AwardedProduct Certification
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: ≤2.73h 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:What does the turnkey project include?
A:
The project covers conceptual design, detailed engineering, procurement, installation, commissioning, validation, training, and regulatory compliance for a complete manufacturing facility.
Q:Can the equipment be customized?
A:
Yes, full customization is available including customization from samples, designs, minor adjustments, and flexible customization to meet specific requirements.
Q:What is the production capacity of the tablet press?
A:
The machine can produce up to 260,000 tablets per hour depending on the model and configuration.
Q:Do you provide after-sales training?
A:
Yes, we provide on-site training for operation, maintenance, hygiene, and safety standards to ensure your personnel can run the facility effectively.
Q:What certifications does the equipment have?
A:
The equipment and projects comply with CE, GMP, and ISO standards, and are designed to meet FDA and EMA regulatory requirements.

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