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Multi-Head Automatic Servo Control Vial Bottling Filler with GMP Standard
US$50,000.00-220,000.00
1 Piece
Product profile
After-sales Service
Field Installation, Commissioning and TrainingCertification
CE, GMP, ISO, GMPCondition
NewModel NO.
customizedCustomized
CustomizedVoltage
380VWarranty
1 YearPump Type
Ceramic Pump, Peristaltic Pump, Metal PumpProcess Type
Washing, Sterilizing, Filling, Stoppering, CappingIndustrial Use
HPLC, Uplc, LC, Gc, LC-Ms, Gc-Ms AnalysisCapacity
CustomizedType
Pharmaceutical Packaging MachineryFinished Dosage Form
LiquidPrecision
High PrecisionComputerized
ComputerizedTransport Package
Carton; Wooden Case; Wooden Package;Specification
9620.00cm * 2540.00cm * 2330.00cmTrademark
IVENOrigin
ChinaHS Code
8422303090Production Capacity
CustomizedKey features
GMP Standard Compliance: Meets GMP production standards with closed cleaning operations to prevent contamination.
Full Servo Control System: Adopts PLC and frequency converter for stable, reliable, and precise operation.
Flexible Pump Options: Ceramic, peristaltic, or metal pumps available to ensure high filling accuracy.
SS 316L Material Contact: Product contact parts use superior SS 316L to ensure cleaning and eliminate dead angles.
Smart Safety Features: Includes no-vial-no-filling logic and automatic rejection of unqualified vials.
Data Integrity & Audit: Industrial PC control supports audit trails, data integrity, and remote access.
Customized Capacity: Production capacity is fully customizable to meet specific client requirements.
Comprehensive After-Sales: Includes field installation, training, and engineer dispatch for 6-12 months.
Company profile
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.
Product Q&A
Q:Where have you exported your equipment?
A:
We've already exported to more than 45+ countries in Aisa, Europe, Middle East, Africa, South America,etc.
Q:Can you arrange the visit to your user?
A:
Yes. We can invite you to visit our turnkey projects in Indonesia, Vietnam, Uzbekistan, Tanzania etc.
Q:Can you customize the machine according to our requirements?
A:
Yes.
Q:Is your equipment in accordance with GMP, FDA, WHO?
A:
Yes, we will design and manufacture the equipment according to the requirement of GMP/FDA/WHO in your country.
Q:What is your payment terms?
A:
Generally, TT or irrevocable L/C at sight.
Send Inquiry
*To:
Shanghai Iven Pharmatech Engineering Co., Ltd.
Shanghai Iven Pharmatech Engineering Co., Ltd.*Content:
Supplier replies will be sent to your registered email
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