Have you done similar projects overseas?

Our scope covers more than 100 countries and regions around the world, such as the USA, Japan, Australia, Germany, Spain, Greece, Hungary, Russia, Ukraine, Uzbekistan, India, Bangladesh, Vietnam, Thailand, Iran, Jordan, Saudi Arabia, Argentina, Brazil, Mexico, Colombia, Egypt, Tunisia, North Korea, and others. Including Sanofi-Aventis, Wyeth, Herbalife, Stada-Hemofarma, Teva, Ovaltine, Baxter-Claris, Otsuka, and other international companies.HM Pharmachine Group has become the Reputed Turnkey So

Do you have a professional engineering team for installation and supervision on-site?

Yes, of course. We have engineer team to work overseas with rich experience.

What documents will you provide?

We will provide IQ, OQ, DQ, FAT, SAT, operation manual, drawings, etc.

What are your advantages?

More than 20 years of professional experience Design, Manufacturing & Turnkey Project One-stop Technical Service High Quality + Economical Solution

Low Residue OEM Custom All-in-One Liquid Vial Filling Machine

Name: Low Residue OEM Custom All-in-One Liquid Vial Filling Machine
Brand: HM Pharmaceutical Engineering & Project (Zhejiang) Co., Ltd.
SKU: 2298093495

Zhejiang, ChinaHM Pharmaceutical Engineering & Project (Zhejiang) Co., Ltd.

US$20,000.00-50,000.00

1 Piece

Product profile

Customization

Available

Certification

Condition

New

Model NO.

HM VFill Series

Customized

Fill Range

100-249ml

Filling Principle

Piston Filling

Machine Type

Ampoule Filling Machine

Main Material

Stainless Steel

Voltage

220V

Product Name

Hm Vfill Aseptic Vial Filler Monoblock

Process Steps

Fill + Stoppering + Cap Crimping

Filling Products

Injectable Liquid and Powder Vials

Construction Material

316L Stainless Steel

Design Standard

Aseptic Sanitary, cGMP Standard

Aseptic Integration

Class a Laf / Rabs Compatible

Control System

Siemens PLC

HMI System

Siemens HMI Touch Screen

Drive System

Servo Motor Driven

Speed Adjustment

HMI Speed Setup and Regulation

Compliance

USA FDA 21 CFR Part 11 Ready

Transport Package

Seaworthy Packing

Specification

Standard Specifications or Customized

Trademark

Origin

Zhejiang, China

Production Capacity

1 Year/12 Months

Key features

Aseptic Monoblock Design: Integrates filling, stoppering, and capping in one cGMP-compliant system with 316L stainless steel.

FDA 21 CFR Part 11 Ready: Ensures data integrity and electronic record compliance for regulated pharmaceutical factories.

Versatile Filling Capability: Handles both injectable liquid and powder vials with support for lyophilized and non-lyophilized processes.

Smart Reject-Prevention Logic: Features no-vial-no-action logic to prevent incomplete packaging and reduce product loss.

Flexible Production Capacity: Output options range from 10-50 to 30-100 vials per minute for scalable production needs.

Advanced Control System: Equipped with Siemens PLC and HMI touch screen for precise speed setup and regulation.

Global Project Experience: Served over 100 countries with major clients including Sanofi, Wyeth, and Baxter-Claris.

Comprehensive Documentation: Provides IQ, OQ, DQ, FAT, SAT, operation manuals, and technical drawings for full compliance.

Company profile

Importers and ExportersYears of Export Experience

HM Pharmaceutical Engineering & Project (Zhejiang) Co., Ltd.

Zhejiang, China

Business Type: Manufacturer/FactoryExport Year: 1999-03-18Nearest Port: SHANGHAI,CHINA, NINGBO ,CHINAAverage Response Time: ≤0.19hTerms of Payment: LC, T/T, D/P, etc.International Commercial Terms(Incoterms): FOB, CFR, CIF

AI-Powered supplier vetting

SummaryHM Pharmachine Group presents evidence of established manufacturing, export, and customization capabilities. It operates three production lines, has 6–10 quality-control staff, reports 11–20 years of R&D engineer experience, and has exported for 16 years to broad international markets. Its management-system certifications include ISO9001:2015, ASME, and GMP. Customization is offered from samples, designs, and through full customization, supported by CAD and PORTAL tools and documented R&D inputs, outputs, reviews, verification, and validation. However, important gaps remain: no approved-supplier list, written corrective-action or complaint-handling procedures, valid manufacturing-capacity contracts with related subcontractors, overseas warehouse or showroom capability, environmental-impact assessment report, or available SDK. Financial information is represented only by years rather than performance metrics, so credibility cannot be judged. Customer references are stated, but Fortune 500 collaboration is...

Supplier typeThe supplier is presented as a manufacturing and turnkey project provider for machinery, including ALU cutters, drilling, engraving, lathe, and panel-cutting equipment. It operates three production lines, serves broad international markets, and describes itself as a turnkey solution provider.

CertificationsThe supplier reports ISO9001:2015 certification, with ASME, ISO 9001, and GMP also listed among its management-system certifications. This is explicit evidence of multiple relevant certifications, although the slices do not provide certificate scope or validity details for each item.

After-Sales capabilityThe supplier has in-stock service capacity, overseas agents or branches, and trade-show participation, but it has no written procedures or records for corrective/preventive actions or customer complaint handling. Finished-product inspection instructions exist without written records, indicating a documented-service weakness.

Production capacityThe supplier reports three production lines, in-stock service capability, a broad machinery facility, and 2–3 month lead times in both peak and off-peak seasons. Nevertheless, it lacks a valid contract governing manufacturing capacity with its related subcontractor, which is a stated capacity-management deficiency.

Customization capabilityCustomization is explicitly available from samples, customer designs, and through full customization. The supplier also reports R&D personnel, CAD and PORTAL tools, and documented design-development controls, providing direct support for customization capability.

Product Q&A

Q:Are you a manufacturer or trader?

We are a manufacturer. Our factory is located in Zhejiang Province.

Q:What certificate do you have?

We have CE, ISO, ROHS, SGS, etc.

Q:What is the production lead time?

Standard 60-120 days after deposit received and technical data for the cleanroom project, Standard 60-150 days after the deposit is received, and technical data is confirmed based on different pharmaceutical machines.

Q:What are the International Commercial Terms accepted?

We have done various terms like FOB, CIF, CFR, EXW, DDU, DDP, CIP, etc., and we have a professional team to handle the shipping and a professional shipping partner.

Q:What are the payment terms?

T/T, L/C, PayPal, Western Union, Alipay, etc. It's flexible.