What is the minimum order quantity?

The minimum order quantity is 1 set.

What certifications does the equipment hold?

The equipment holds CE, GMP, and ISO certifications.

What is the lead time for production?

The average lead time is 1-3 months, varying by season.

Total Solution for Solid Dose Production Line/Full-Service OSD Manufacturing Provider

Name: Total Solution for Solid Dose Production Line/Full-Service OSD Manufacturing Provider
Brand: Shanghai Iven Pharmatech Engineering Co., Ltd.
SKU: 1933017191

Shanghai, ChinaShanghai Iven Pharmatech Engineering Co., Ltd.

US$200,000.00-600,000.00

1 Piece

Product profile

Certification

CE, GMP, ISO

Warranty

Field Installation, Commissioning and Training

Production Capacity (Kg/Batch)

15/30--300/500

Model NO.

customized

Dimension(LWH)

1.5*1.3*5m--3.5*3.5*10m

Vessel Volume(L)

45-1530

Fan Power(Kw)

7.5-75

Electric Heating Power(Kw)

30-120

Steam Consumption(Kg/H)

180-677

Weight of Mian Machine(Kg)

800-3500

Finished Dosage Form

Granules

Precision

High Precision

Voltage

380V

Computerized

Customized

Condition

New

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

Full Turnkey Solution: Complete design, procurement, installation, and training for oral solid dosage manufacturing.

Regulatory Compliance: Facilities designed to meet FDA and EMA standards with full validation support.

Customizable Capacity: Production capacity ranges from 15 to 500 kg per batch based on specific needs.

High Precision Output: Ensures consistent, high-quality granules with advanced precision control systems.

Expert Technical Support: Field installation, commissioning, and training provided by experienced engineers.

Cost & Time Efficiency: Streamlined process reduces setup time and costs associated with individual sourcing.

Flexible Customization: Offers full customization from samples or designs to match unique manufacturing goals.

CE & GMP Certified: Equipment meets international safety and quality standards including CE and GMP.

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: ≤1.46h 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.