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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
Place of Origin Shenzhen,Guangdong
Nombre de la marca HJW
Certificación ISO 14001,ISO 9001,CE,EPA
Minimum Order Quantity 1set
Precio US$14700~US$15000
Packaging Details export standard wooden case
Delivery Time 1-7working days(depand on raw materials stocking)
Payment Terms L/C,D/P,T/T,Western Union
Supply Ability >300sets/month

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Datos del producto
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
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Descripción de producto

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 )



Etiquetas:

Sistemas de ultrafiltración industrial

Equipo de la ultrafiltración

El sistema de