The storage and transport process in logistics is affected in individual process steps by quality risks of varying levels, which must be adequately managed. These critical influencing factors can be minimised through qualification and validation activities, which can also verify compliance with the GxP requirements.
With the help of well-structured risk management, the quality assurance measures can be directed, the focus set on the critical aspects of the storage and transport process, thus optimising the quality assurance efforts.
We support our customers in assuring their GDP & GSP compliance - from specialized pharmaceutical logistics specialists to the logistics departments of pharmaceutical companies up to the transfusion medical storage areas of clinics.
