Does the equipment comply with GMP standards?

Yes, the equipment complies with cGMP, GAMP5, and FDA regulations, ensuring high reliability and precision for pharmaceutical and biological industries.

What are the main features of the SCADA system?

The computer-based SCADA system complies with GAMP regulation, saves up to thousands of recipes, and allows data recording via tables or curves for preservation.

Pharmaceutical Lyophilizer Price 150L Loading Capacity for Biological Products

Name: Pharmaceutical Lyophilizer Price 150L Loading Capacity for Biological Products
Brand: Zhejiang Lyomac Pharmaceutical Equipment Co., Ltd.
SKU: 1979602445

Zhejiang, ChinaZhejiang Lyomac Pharmaceutical Equipment Co., Ltd.

US$9,500.00-10,000.00

1 Set

Sample price:US$10000.00/set.Request sample

Product profile

Customization

Available

After-sales Service

Provided

Warranty

Provided

Model NO.

LYOPRO-7.5

Movement Way

Fixed

Flow

Cross Flow

Heating Mode

Convective

Material Status

Solution

Drying Medium

Effluent Gas

Operational Method

Continuous

Type

Continuous Vacuum

Drying Capacity

150

Shelf Area

7.56

Transport Package

Provided

Specification

5000*1750*2400

Trademark

LYOMAC

Origin

China

Production Capacity

1/Three Month

Key features

cGMP and FDA Compliance: Complies with cGMP, GAMP5, and FDA regulations for pharmaceutical and biological production.

Advanced SCADA Control: Computer-based SCADA system saves up to thousands of recipes and records data via tables or curves.

Energy Saving Function: Features motor switch over, inverter control, and eutectic online determine function for efficiency.

Flexible Layout Design: Flexible arrangement design suits user's plant layout, saving space and ensuring easy installation.

Global After-Sales Network: Service network all over the world with preventive maintenance and AMC service for the machine's life.

150L Pilot Scale Capacity: Pilot model with drying capacity up to 150 Liters, covering most demands for vial or material production.

Automatic Operation: Includes automatic shelf stoppering under vacuum, SIP, and CIP systems for streamlined operation.

Company profile

Zhejiang Lyomac Pharmaceutical Equipment Co., Ltd.

Zhejiang, China

CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service Available CertifiedCustomization Options: Customization from Samples CertifiedExport Year: 7 Years CertifiedNearest Port: Shanghai Port, Ningbo PortAverage Response Time: ≤24h

AI-Powered supplier vetting

SummaryThe supplier is a China-based limited company offering vacuum freeze dryers. Evidence identifies Zhejiang Lyomac Pharmaceutical Equipment Co., Ltd., established in 2018, with 14 employees in one record and 17 in another. It holds an ISO9001:2015 certificate, while another description also references TUV-CE and ISO9001 certification. The supplier reports private mold design, 3D software design, SDK availability, professional technical supplier status, and sample-based customization. Manufacturing contracts with associated subcontractors are in place, and more than 10 production lines are reported, although lead-time information is inconsistent. Overseas services include installation, debugging, training, and repair. Documented procedures exist for supplier assessment, corrective actions, and complaints, but records are absent. Financial-period data is provided, but no financial figures or explicit financial assessment are available. No customer cases, inventory capability, overseas warehouse, or showroom...

Supplier typeThe supplier is identified as a limited company from China, offering vacuum freeze dryers. It is reported as independent of a larger company group, although the records show different employee counts and locations.

CertificationsThe supplier explicitly reports an ISO9001:2015 certificate, and its company description additionally references TUV-CE and ISO9001:2000 certification. These statements support established quality-system certification, though the validity and scope of the additional certifications are not independently documented.

After-Sales capabilityOverseas services include equipment installation, debugging, training, and repair, and a valid manufacturing contract exists with each associated subcontractor. However, service-management, corrective-action, and complaint procedures have no written records; the supplier also reports no overseas warehouse or showroom.

Production capacityThe supplier reports more than 10 production lines, valid manufacturing contracts with associated subcontractors, and broad international export markets. Capacity assessment is constrained by inconsistent lead-time records: one source states 4–6 months off-season, while another states one month off-season and gives an unclear peak-season entry.

Customization capabilityThe supplier explicitly provides customization from samples and reports private mold design and 3D software design services. These statements directly support the ability to develop customized products based on customer samples.