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End-to-End Pharmaceutical / Medical OSD Manufacturing Solution with GMP Standard
US$130,000.00-280,000.00
1 Piece

Product profile

Application

Pharmaceutical Food Industries;Medical;

Certification

CE, GMP, ISO

Control System

Fully Automatic

Model NO.

customized

Customized

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

Condition

New

Warranty

1 Year

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 GMP Solution: Complete end-to-end pharmaceutical manufacturing facility design and setup compliant with GMP standards.
High Precision Tablet Press: Features high-accuracy automatic powder suction and tablet pressing with capacities up to 260,000 tablets/hour.
Comprehensive Customization: Offers full customization, minor customization, and flexible options based on client samples or designs.
Full Project Stages: Includes conceptual design, detailed engineering, procurement, installation, commissioning, validation, and training.
Regulatory Compliance: Facilities designed to meet FDA and EMA guidelines ensuring consistent product quality and safety.
Video Technical Support: Post-warranty service includes video technical support for troubleshooting and maintenance guidance.
Core Component Quality: Utilizes high-quality motors and engines as core components for reliable machine performance.
Outgoing Inspection: Provides video outgoing inspection to ensure product quality before shipment to the client.

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: ≤2.28h 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, qualification, validation, training, and regulatory compliance.
Q:Is the manufacturing solution customizable?
A:
Yes, we offer full customization, minor customization, and flexible options based on client samples or designs.
Q:What certifications does the facility meet?
A:
The solution is designed to meet GMP standards and regulatory guidelines from authorities like the FDA and EMA.
Q:What is the warranty period?
A:
We provide a 1-year warranty for the equipment.
Q:What after-sales services are available?
A:
Services include field installation, commissioning, training, and video technical support after the warranty period.

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