EMA’s IDMP-SPOR Implementation Guideline v2.1.1

EMA’s IDMP-SPOR Implementation Guideline v2.1.1

Identification of Medicinal Products (IDMP) standards were developed by the ISO to specify the use of standardised definitions for the identification and description of medicinal products for human use. In this article, we provide an overview of the latest IDMP v2.1.1 guideline and summarise that, given the scope of changes, it is relatively low impact to the regulatory profession.

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