In the pharmaceutical sector, computerized systems are subject to strict requirements. For quality and security reasons, each system that is used must be validated and must then be revalidated at regular intervals and when any changes are implemented. The development of relevant tools underpins not only our expertise in this area, but it also provides you with support when you create validation documentation. We work on the basis of the GAMP 5 recommendations here.

Within our international partner network, we also have access to further experts in this field, who we use on a project-specific basis.