About this event
All EMA marketing authorization holders have to be ready by 2023 to meet IDMP requirements. This implementation goes beyond a regulatory compliance project and can become a global stake for the company.
The IDMP standard (Identification of Medical Products) has been developed to improve exchanges on medicinal product data during the product lifecycle and to enhance the interoperability with the European agency. However, these data today constitute a considerable volume and are scattered in multiple locations, in a format often hardly usable (PDFs, foreign language, unstructured Excel files, etc.). Oresys organizes a webinar to outline how to transform this requirement into an opportunity. This event will address the following issues:
Responsable de la Data Science
Cabinet de conseil indépendant et acteur majeur du conseil en management, organisation et systèmes d’information.
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