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Ultrafiltration Membrane Filter For Separation Of Pharmaceutical Industry 5TPH Water Treatment System
Ultrafiltration Membrane Filter For Separation Of Pharmaceutical Industry 5TPH Water Treatment System
Specifications
Brand Name :
HJW
Certification :
ISO 14001,ISO 9001,CE,EPA
Place of Origin :
Shenzhen,Guangdong
MOQ :
1set
Price :
US$14700~US$15000
Payment Terms :
L/C,D/P,T/T,Western Union
Supply Ability :
>300sets/month
Delivery Time :
1-7working days(depand on raw materials stocking)
Packaging Details :
export standard wooden case
Capacity :
5m³/H（Customizable)
Membrane Material :
RC, PES
Operating Pressure :
0.5–3 bar
Core process :
UF,RO,UV
Operation model :
PLC control
Verified :
GMP/FDA/EMA
Description

I.Overview
Ultrafiltration (UF) equipment plays a key role in the pharmaceutical industry for separation, purification, concentration and pyrogen removal to meet the high purity requirements of drug manufacturing.
The core values are: high purity assurance (removal of pyrogens, viruses, impurities, compliant with pharmacopoeia standards),
process flexibility (applicable to a wide range of products such as antibodies, vaccines, gene therapy, etc.), and design for compliance (meets the stringent validation requirements of GMP/FDA/EMA).


II.Typical Process Flow


Monoclonal Antibody (mAb) Purification:
Cell Culture Solution → Centrifugation/Deep Filtration → Ultra Filtration (30 kDa) → Protein A Chromatography → Viral Filtration → Ultra Filtration Dialysis (Liquid Exchange) → Preparation


Water for Injection (WFI) for pyrogen removal:
purified water → multi-effect distillation / RO → ultrafiltration (10 kDa) → UV disinfection → storage and distribution


Concentration of viruses for vaccine production:
Virus culture solution → microfiltration (0.22 μm) → ultrafiltration (300 kDa) → sucrose gradient centrifugation → inactivation/freeze-drying


III.Core Attribute Parameters

Performance Requirements for Ultrafiltration Membranes (Pharmaceutical Grade)
Parameter Pharmaceutical Grade Standard Description
Membrane Material Regenerated Cellulose (RC), PES RC: Low protein adsorption; PES: Resistant to acid-base cleaning.
Molecular Weight Cut-Off (MWCO) 1–300 kDa Antibody purification: 100 kDa; Pyrogen removal: 10 kDa.
Flux (LMH) 20–100 (Adjusted by Viscosity) High-viscosity feed (e.g., DNA) requires low flux.
Operating Pressure 0.5–3 bar Tangential Flow Filtration (TFF) mode reduces concentration polarization.
Integrity Test Bubble Point Test ≥3 bar Ensure membrane integrity; meet GMP validation requirements.
Key Quality Control Indicators
Application Output Standard Regulatory Basis
Pyrogen Removal for Injections <0.001 EU/mL Chinese Pharmacopoeia 2020 Edition
Blood Products Viral Reduction ≥4 log (99.99%) FDA/EMA Viral Safety Guidelines
Biologics HCP ≤5 ppm ICH Q6B Quality Standar


IV.Core Application Areas
Biologics Purification
Blood Products Processing
Injectable Pyrogen Removal
Enzyme Concentration
Chinese Medicine Modernization


V.Here is a guideline for you to get a proper quotation
Tell us the raw water/source of water(tap water, well water, or sea water, etc)
Provide water analysis report(TDS , conductivity, or resistivity, etc)
Required production capacity( 5m³/H, 50m³/H,or 500m³/H, etc)
What's the pure water used for( industrial,Food and Beverage,or agriculture, etc )



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Ultrafiltration Membrane Filter For Separation Of Pharmaceutical Industry 5TPH Water Treatment System

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Product Detail
Brand Name :
HJW
Certification :
ISO 14001,ISO 9001,CE,EPA
Place of Origin :
Shenzhen,Guangdong
MOQ :
1set
Price :
US$14700~US$15000
Payment Terms :
L/C,D/P,T/T,Western Union
Contact Supplier
Ultrafiltration Membrane Filter For Separation Of Pharmaceutical Industry 5TPH Water Treatment System

Shenzhen HongJie Water Technology Co., Ltd.

Verified Supplier
1 Years
shenzhen
Since 2013
Business Type :
Manufacturer
Main Products :
Pure Water Equipment, Ultrapure Water Equipment, Reverse Osmosis Systems
Total Annual :
25000000-30000000
Employee Number :
180~200
Certification Level :
Verified Supplier
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