Collection, systematic documentation and evaluation of all necessary information in connection with indications of drug risks, in particular adverse drug reactions, interactions and contraindications, as well as indications of quality defects, misuse, long-term use, abuse or counterfeit drugs * Passing on necessary information to pharmacovigilance departments at service providers, licensees/licensors, distribution partners and affiliates within the framework of contractual pharmacovigilance agreements * Support in creation and maintenance of pharmacovigilance system master file (PSMF) * Overview of the pharmacovigilance system including the establishment of suitable key performance indicators to measure quality
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