What is the minimum order quantity?

The minimum order quantity is 1 Set, allowing for flexible procurement for different project scales.

How long is the average lead time?

The average lead time is one month during the off-season and one to three months during the peak season.

What payment terms are accepted?

We accept various payment terms including LC, T/T, D/P, PayPal, Western Union, and small-amount payments.

Total Solid Dosage Formulation Project Pharmaceutical & Medical Turnkey with GMP

Name: Total Solid Dosage Formulation Project Pharmaceutical & Medical Turnkey with GMP
Brand: Shanghai Iven Pharmatech Engineering Co., Ltd.
SKU: 2080035155

Shanghai, ChinaShanghai Iven Pharmatech Engineering Co., Ltd.

US$200,000.00-800,000.00

1 Piece

Product profile

Certification

CE, GMP, ISO, GMP

Customized

Feature

High Working Efficiency

Model NO.

customized

Raw Material

304/316ss

Key Selling Points

Easy to Operate;Long Service Life

Roller and Feed Speed Regulation Type

Electromagnetic Speed/Variable Frequency Speed Con

Video Outgoing-Inspection

Provided

Roll Size(mm)

Customized

Roll Speed(Rpm)

Customized

Core Components

PLC, Motor, Pressure Vessel

Roller Pressure

20MPa

Finished Dosage Form

Granules

Precision

High Precision

Voltage

380V

Computerized

Condition

New

Warranty

Field Installation, Commissioning and Training

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

Comprehensive Turnkey Solution: Complete package including facility design, equipment procurement, installation, and training for seamless setup.

GMP & Regulatory Compliance: Facility designed to meet FDA/EMA standards with CE, GMP, and ISO certifications ensuring quality and compliance.

High Working Efficiency: Features electromagnetic speed regulation and variable frequency speed control for optimized production performance.

Flexible Customization Options: Offers full customization, minor customization, and flexible options from samples or designs to meet specific needs.

Cost and Time Savings: Streamlined project management reduces costs through bundled pricing and accelerates market entry via faster deployment.

Professional Training Support: Includes field installation, commissioning, and comprehensive training for customer personnel on operation and maintenance.

High Precision Manufacturing: Utilizes PLC, motor, and pressure vessel core components to ensure high precision in producing oral solid dosage forms.

Durable 304/316 Stainless Steel: Constructed with 304/316 stainless steel raw materials for long service life and hygiene in pharmaceutical applications.

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: ≤2.89h 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?

The turnkey project includes a complete package of facility design, equipment procurement, installation, commissioning, and training, allowing clients to start operations immediately upon handover.

Q:What certifications does the equipment have?

The equipment and project comply with CE, GMP, and ISO certifications, ensuring adherence to international pharmaceutical manufacturing standards.

Q:Is customization available for this project?

Yes, we offer flexible customization options including full customization, minor customization, and customization from samples or designs to suit specific client requirements.

Q:What is the warranty and after-sales service?

We provide field installation, commissioning, and training as part of the warranty and after-sales service to ensure proper operation and maintenance.

Q:What are the main markets for this product?

Our main markets include North America, Europe, Southeast Asia/Mideast, and Africa, serving pharmaceutical companies globally.