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Chromatography columns

With almost 40 years of unrivalled experience in process-scale chromatography, GE Healthcare supplies a wide range of columns to meet the demands of modern biopharmaceutical manufacturing, and extract the highest performance from our BioProcess™ Media.

AxiChrom™ columns - for process development and full-scale manufacturing
AxiChrom™ columns - for process development and full-scale manufacturing

AxiChrom columns introduce three key features – Intelligent Packing, Intuitive handling, and Predictable scale-up – that together make process chromatography easier, safer, and more efficient.

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BPG™ columns -  for small-scale GMP production
BPG™ columns - for small-scale GMP production
  • Glass columns used in process development and small scale biopharmaceutical manufacturing
  • Pressure rating up to 8 bar
  • Scalable from 100 mm to 450 mm diameter
  • All materials carefully selected for safety and biocompatibility
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Chromaflow™ columns - for large-scale GMP production
Chromaflow™ columns - for large-scale GMP production
  • Well established process-scale columns for capture or intermediate purification
  • Scalable up to 2000 mm diameter
  • Pressure rating 3 bar
  • Pack-in-place with patented nozzle technology
  • Customized columns available
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FineLINE™ columns - process development and small-scale GMP production
FineLINE™ columns - process development and small-scale GMP production
  • Stainless steel columns (35 mm tube in glass)
  • Pressure rating 20 bar
  • Scalable from 35 mm to 350 mm diameter
  • Specially developed for SOURCE™ media
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INdEX™ columns - simple and versatile columns for process development
INdEX™ columns - simple and versatile columns for process development
  • Scaleable from 70 to 200 mm with tube heights up to 950 mm
  • Bed heights from 30 to 610 mm
  • Pressure rating 3 bar
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ReadyToProcess prepacked columns - for purification of biopharmaceuticals for clinical phase I and II studies
ReadyToProcess™ prepacked columns - for purification of biopharmaceuticals for clinical phase I and II studies
  • Time savings by making several time-consuming steps redundant
  • Cost savings by lowering buffer consumption and reducing cleaning validation demands
  • Process security in terms of robust column performance
  • Scalability to facilitate conventional approach in larger scale
  • No cross-contamination problems
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