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GMP Compliant Water Purification System for Pharmaceutical Line
US$20,000.00
1 Piece

Product profile

Customization

Available

Certification

ISO9001

Salt Rejection Rate

1

Model NO.

1000L/H

Application

Industry

Capacity

19000L

Applicable Industries

Pharmaceuticals Laboratories Hospitals

Does It Support Inspection

Yes

Does It Support Customization

Yes

Electrical Control System Brand

Siemens

Transport Package

Wooden Case

Specification

304

Trademark

WEMAC

Origin

Weifang Shandong

Production Capacity

1/30days

Key features

GMP & 21 CFR Compliance: Supports electronic signatures and records for GAMP 5 and 21 CFR Part 11 audit tracking.
Modular & Compact Design: Features a compact structure with an aesthetically pleasing layout for easy operation and maintenance.
Advanced PLC Control: HMI+PLC full-automatic control with multi-level security and diverse communication modes.
High-Quality Welding: Stainless steel pipes use gas-protected automatic welding with electrochemical polishing for durability.
Energy Efficient Operation: Variable frequency control reduces energy consumption and minimizes microbial growth during standby.
Dual Softener System: Pre-treatment features dual softeners with automatic regeneration for 100% continuous water supply.
Comprehensive Documentation: Provides endoscope photos, pressure test reports, and passivation reports for quality verification.
Customizable Capacity: Output is customizable, with a reference capacity of 3000L/H for flexible industrial applications.

Company profile

Shandong Eagle Pharma Machinery Co., Ltd.
In-stock CapacityQuality AssuranceR&D CapabilitiesFull Customization
Business Type: Manufacturer/Factory, Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service AvailableAverage Response Time: ≤2.53h

AI-Powered supplier vetting

SummaryThe supplier is identified as a trading company with a broad technical, equipment, software, and engineering-related business scope. It demonstrates professional technical R&D positioning, 3D software design, ODM, OEM, and multiple customization options. Quality and service procedures are partly established, including inspection instructions, complaint handling, supplier assessment, and corrective-action records. However, the supplier has only one quality inspector, has exported for one year, lacks raw-material traceability labels and written quality records, and has no overseas warehouse or showroom. Innovation evidence is mixed because no new products were reported in the past year and no SDK is available. Financial information is present only as year references, without sufficient evidence to assess credibility.
Supplier typeThe supplier is explicitly classified as a Trading Company. Its stated scope covers technical services, technology development, equipment sales, software development, IoT services, industrial engineering design, and equipment repair, indicating a technically oriented trading and service business rather than a clearly documented manufacturer.
After-Sales capabilityThe supplier has documented and followed procedures for complaint handling, supplier service-capability assessment, and corrective/preventive actions, and it reports in-stock service capability. However, it lacks overseas warehouse and showroom capabilities, so the evidence supports structured service handling but not comprehensive overseas support.
R&D capabilityThe supplier reports professional technical R&D capability, 3D software design, ODM services, and OEM services for popular brands. Counterbalancing this, it reported no new products during the past year and has no available SDK, so the evidence supports design and development services but not strong recent product innovation.
Customization capabilityThe supplier explicitly provides customization from samples, full customization, and customization from customer designs. It also offers 3D software design and ODM services, providing clear evidence of broad customization capability.

Product Q&A

Q:Is the system compliant with GMP and FDA standards?
A:
Yes, the system supports electronic signatures and records to ensure compliance with GAMP 5 requirements and 21 CFR Part 11.
Q:What is the output capacity of the water purification system?
A:
The reference output is 3000L/H, but the capacity is customizable to meet specific industrial needs.
Q:What materials are used for the pipes and fittings?
A:
The main material is 316L stainless steel. Pipes are stretch-bent to minimize welding, and welds are gas-protected and polished.
Q:Does the system support automatic operation?
A:
Yes, it features HMI+PLC full-automatic control with automatic program management for operation, backwashing, and regeneration.
Q:Can the system be customized for pharmaceutical laboratories?
A:
Yes, the system supports customization and is applicable to pharmaceuticals, laboratories, and hospitals.

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