European Union International Organization for Standardization (ISO) for the identification of medici
The European Union (EU) International Organisation for Standardization (ISO) identification of medical products (IDMP) / Substance, Product, Organisation and Referential (SPOR) data Task Force meeting with representatives from the European Medicines Agency, national competent authorities, pharmaceutical industries associations, terminology organisations, software vendors and developers of medicinal products dictionaries / databases discusses 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.
