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Regulatory Support

Biologics cGMP Manufacturing

Regulatory Affairs

We provide regulatory support to drive your products through clinical development, registration and market launch.

Our regulatory affairs services will verify the suitability of the production process, product specifications and analytics to meet your regulatory milestones according to each stage of development.

We will support your writing of the Common Technical Document for submission. We will also ensure that all audit or inspection by in-licensing companies or regulatory bodies will go smoothly.


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

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

View Map | GPS: Latitude: 50.5932225 - Longitude: 5.5606055

Download our Eurogentec Biologics profile

Technical inquiries

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

GMP Biologics Information Request

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