Korte beschrijving
It involves the acquisition of a computerised system that is able to acquire, store, process, report and produce information and data required or generated during the processes that are currently in place for the production, certification and distribution of radiopharmaceuticals. The purpose of this system is to create a paperless environment that supports and improves the current GMP quality management system, elevating it to a level where it can conform to present-day standards set for quality, regulatory compliance and product safety, resulting in full traceability.