Date
- Thursday, 30 June 2016, All day
Location
- European Medicines Agency, Amsterdam, the Netherlands
European Union (EU) International Organisation for Standardization (ISO) identification of medical products (IDMP) task force meeting with the representatives from the European Medicines Agency (EMA), terminology organisations, software vendors and developers of medicinal products dictionaries / databases to discuss aspects of planning, development, implementation and maintenance of the ISO IDMP standards in the EU, in line with requirements defined at international level and based on agreed EU implementation principles.