Data on medicines (ISO IDMP standards): research and development
HumanData on medicines
Swedish is available via eTranslation, the European Commission's machine translation service.
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The European Medicines Agency (EMA) is in the process of implementing the standards developed by the International Organization for Standardization (ISO) for the identification of medicinal products (IDMP).
EMA is implementing the standards in a phased programme based on the four domains of master data in pharmaceutical regulatory processes: substance, product, organisation and referential (SPOR) master data.