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Purification

cGMP Manufacturing

Purification

A dedicated, experienced staff takes care of your product in three independent purification suites, applying the principles of segregation to prevent cross contamination:
  • Separated and dedicated HVAC system for each production suite (100% fresh air supply, non-recirculating)
  • Clean areas of Grade C (10.000)
  • Appropriate waste treatment
  • Validated CIP cycles for process equipments

Qualified downstream equipments and techniques consist of:
  • chromatography rigs
  • ultra/diafiltration systems
  • centrifugation
  • crystallization
  • precipitation
  • extraction
  • coupling
  • labeling
  • cleavage

These (and others) allow the purification of your product according to the process defined and transferred by the PT&D Department.

Facilities are designed to prevent cross contamination and guarantee the highest quality level:

Our cGMP fermentation teams work in close collaboration with our development staff to perform scaling-up from a wide range of cell types. They are continuously trained to operate in full compliance with the cGMP.

Office

Kaneka Eurogentec S.A. Biologics Division
LIEGE Science Park
Rue du Bois Saint Jean, 14
4102 Seraing
BELGIUM

Tel.: +32 4 372 74 00
Fax: +32 4 365 16 04

info.biologics@eurogentec.com

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Download our Eurogentec Biologics profile

Technical inquiries

Pascal Bolon, Ph.D.
Biologics Sales & Marketing Manager

GMP Biologics Information Request

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