Joint European Medicines Agency/Drug Information Association information day on International Organization for Standardization identification of medicinal products standards: achieving compliance

Date: 23/06/2015
Location: European Medicines Agency, London, UK
This information day is primarily aimed at providing stakeholders with information to help prepare for the business change to come and at sharing the vision of common European Union (EU) strategy for the International Organization for Standardization (ISO) identification of medicinal products (IDMP) standards implementation in response to a worldwide demand for internationally harmonised specifications for medicinal products. Topics to be addressed relate to background of the IDMP standards and legislation, structure of the IDMP standards, international stakeholders perspective and identification of future direction. This forum is providing opportunity to understand requirements, identify key challenges and to exchange views between regulators, industry, system developers and other stakeholders. Places limited.

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