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Membrane Filtration Equipment for Pharmaceutical Industry, Standard Compliant Design

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Product Spotlights

ZLN Membrane Filtration Equipment is designed for pharmaceutical compliance with sanitary SS316L construction, interchangeable UF/NF/RO modules, and automated CIP/SIP capability. Trusted by global pharma companies, our scalable solutions deliver high purity, low energy consumption, and easy validation support.
US$ 200000 - 1000000 MOQ: 1 Set
Key Specifications
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Material:
Stainless Steel 316L / 304 (optional)
Membrane Type:
UF / NF / RO / MF (customizable)
Membrane Area:
0.5 – 200 m² (per module)
Payment & Shipping
Payment Methods:
Port of Shipment:
Shanghai
Delivery Detail:
30 days
Material Stainless Steel 316L / 304 (optional)
Membrane Type UF / NF / RO / MF (customizable)
Membrane Area 0.5 – 200 m² (per module)
Operating Pressure Up to 40 bar (580 psi)
Operating Temperature 5 – 85 °C (41 – 185 °F)
Flow Rate 100 – 10,000 L/h (customizable)
Application API purification, WFI, water for injection, concentration
Design Standard Compliant with cGMP & FDA guidelines (design level)
Control System PLC + HMI touchscreen (optional)
Sanitary Connections Tri-clamp / DIN / SMS (available)

Tianjin ZhuoLiNeng (ZLN) Technology Co., Ltd. is a professional manufacturer of membrane filtration equipment tailored for the pharmaceutical industry. Our Membrane Filtration Equipment is engineered with a standard compliant design that meets the rigorous requirements of pharmaceutical production, including API purification, water for injection (WFI), and sterile filtration. With over a decade of experience exporting to global markets across North America, Europe, and Asia, ZLN delivers reliable, high-performance filtration solutions that ensure product purity and process efficiency.

This advanced filtration system combines cross-flow membrane technology with sanitary construction, offering seamless integration into existing pharmaceutical lines. Designed to comply with cGMP and FDA guidelines (at design level), the equipment is available in multiple configurations — from lab-scale units to full-scale production modules. Whether you need ultrafiltration for protein concentration or reverse osmosis for high-purity water, our equipment provides consistent, reproducible results.

Key Features & Technical Specifications

  • Sanitary Design: All wetted parts are made of SS316L (or SS304 optional), with electropolished surfaces (Ra ≤ 0.5 μm) to prevent bacterial growth and facilitate CIP/SIP cleaning.
  • Membrane Versatility: Supports Microfiltration (MF), Ultrafiltration (UF), Nanofiltration (NF), and Reverse Osmosis (RO) membranes — interchangeable modules for different separation tasks.
  • Scalable Architecture: Modular design allows easy expansion from 1 to 10+ membrane housings, with membrane area ranging from 0.5 m² to 200 m² per module.
  • Automation Ready: Optional PLC with HMI touchscreen controls pressure, temperature, flow rate, and automatic valve switching for unattended operation.
  • High Recovery: Cross-flow filtration minimizes fouling and achieves up to 95% recovery for water-based streams, reducing waste.
  • Low Energy Consumption: Efficient pump design and optimized membrane channel geometry lower operating costs compared to traditional evaporation or chromatography.
Parameter Range / Option
Membrane Material PES, PVDF, PA, TFC (customizable)
Maximum Operating Pressure Up to 40 bar (580 psi)
Temperature Range 5 – 85 °C (41 – 185 °F)
Flow Rate (per module) 100 – 10,000 L/h
Control System Manual (basic) / PLC + HMI (optional)
Cleaning Method CIP (Clean-in-Place) / SIP (Steam-in-Place) compatible
Connections Tri-clamp (standard) / DIN / SMS / custom

Benefits for Your Pharmaceutical Process

  • Enhanced Product Quality: Membrane filtration provides sharp separation with no chemical additives, preserving the integrity of sensitive APIs and biologics.
  • Compliance Made Easy: Equipment design follows pharmaceutical industry standards, simplifying validation and audit processes for regulatory bodies.
  • Reduced Downtime: Robust construction and easy-to-replace membrane elements minimize maintenance intervals. Automatic CIP cycles can be programmed for overnight cleaning.
  • Flexible Operation: Multiple membrane types and module configurations allow you to switch between concentration, diafiltration, and purification without buying new equipment.
  • Cost Savings: Lower energy consumption compared to thermal processes, plus reduced solvent or chemical usage — leading to a fast return on investment.

Trust ZLN – Your Reliable Partner

As a manufacturer based in Tianjin, China, ZLN has been supplying membrane filtration equipment to pharmaceutical companies worldwide since 2010. Our products have been shipped to North America, South America, Europe, Southeast Asia, Africa, Oceania, the Middle East, and many other regions. We maintain strict quality control at every stage — from raw material inspection to final pressure testing. Each unit is thoroughly tested before shipment, and we provide comprehensive technical documentation including FDS, IQ/OQ protocols, and material certificates upon request.

Our team of experienced engineers can customize the membrane configuration, control system, and ancillary components (such as feed pumps, heat exchangers, and pre-filters) to match your exact process requirements. With a dedicated after-sales support team, we offer remote troubleshooting, spare parts supply, and on-site commissioning services.

Choose ZLN membrane filtration equipment for reliable, compliant, and efficient pharmaceutical separation. Contact us today for a quotation or technical consultation.

Frequently Asked Questions

Q1: What membrane types are available for this equipment?

A: We support Microfiltration (MF), Ultrafiltration (UF), Nanofiltration (NF), and Reverse Osmosis (RO) membranes. The specific type can be selected based on your application — for example, UF for protein concentration, NF for desalting, or RO for WFI production.

Q2: Does the equipment comply with cGMP and FDA regulations?

A: Our design is engineered to meet the requirements of pharmaceutical standards, including cGMP and FDA guidelines (design level). We provide documentation to support your validation efforts, including material certificates, surface finish reports, and assembly drawings.

Q3: Can the system be cleaned in place (CIP)?

A: Yes, the equipment is fully CIP-compatible. It can be equipped with automated CIP skids and programmed cleaning cycles. SIP (steam-in-place) is also available as an option for sterile applications.

Q4: What is the typical lead time for delivery?

A: Lead time depends on the configuration and customization level. Standard units typically ship within 4-6 weeks after order confirmation. For custom designs, lead time may extend to 8-12 weeks. We can provide a precise schedule upon request.

Q5: Do you offer installation and commissioning support?

A: Yes, we offer on-site commissioning services by our experienced engineers, as well as remote guidance via video call. We also provide comprehensive user manuals and training materials.

Q6: How do I select the right membrane area for my process?

A: We can help you calculate the required membrane area based on your feed flow rate, target concentration, and desired throughput. Contact us with your process parameters, and we will provide a customized proposal.

Q7: What are the available payment terms?

A: Common payment terms include T/T (30% deposit, 70% before shipment) and L/C at sight. Other terms may be negotiable for long-term partners.

Q8: Do you provide spare parts and ongoing technical support?

A: Yes, we maintain a stock of common spare parts such as O-rings, seals, and membrane elements. Our technical support team is available via email, phone, or online chat to assist with any operational issues.

Product Tags: Pharmaceutical Membrane Filtration Equipment , Standard Compliant Membrane Filter System , ZLN Pharmaceutical Filtration Unit

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Gold Verified Supplier
1Yr
Verified Business License
Business Type
Manufacturer
Port of Shipment
TianJin
Main Markets
North America, South America, Eastern Europe, Southeast Asia, Africa, Oceania, Mid East, Eastern Asia, Western Europe, Central America, Northern Europe, Southern Europe, South Asia, Domestic Market
Location
Tianjin, China