
Component and equipment processing
Ensure cGMP compliance by preventing cross contamination from components and equipment in contact with the end product
Meeting your unique process requirements in cGMP cleaning and sterilization
Everything that comes in contact with pharmaceutical products must be thoroughly cleaned and sterilized to prevent the risk of contamination. In formulation, fill and finish operations for sterile injectable drug products, global GMP regulations require prevention of cross-contamination via components and equipment that come into contact with the product. All such components and equipment (e.g. machine parts, vessels, etc) must therefore undergo repeatable, validated cleaning and sterilization processes at regular intervals.
Getinge’s portfolio of cGMP washers and sterilizers has been designed to help manufacturers ensure compliance with specific cGMP requirements and process demands.