Their purpose is to facilitate the reliable exchange of medicinal product information in a robust and consistent manner. The ISO IDMP standards specify the use of standardised definitions for the identification and description of medicinal products for human use. ![]() 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).ĮMA is implementing the standards in a phased programme based on the four domains of master datain pharmaceutical regulatory processes: substance, product, organisation and referential (SPOR) master data.
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