Component & Equipment Processing
Ensure cGMP compliance by preventing cross contamination.
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.
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