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Meeting your unique process requirements in cGMP cleaning and sterilization

In biopharmaceutical production, GMP regulations require prevention of cross-contamination of components and equipment such as glass bottles, vials, and machine parts that come in contact with the end product: the drug. The components must be thoroughly cleaned and sterilized at regular intervals, according to specific validated processes.

Getinge’s portfolio of cGMP washers, sterilizers, and closure processing systems (CPS) has been designed to help manufacturers ensure compliance with specific cGMP requirements and process demands.

Dear user, You now see International fallback content. Getinge South East Asia does not review or control this content. It is possible that some of the products on Getinge international are not approved in your country. For more specific  information relevant for your region please contact us.