Europe – Product Management Service (PMS) – Implementation of International Organization for Standardization (ISO) standards for the identification of medicinal products (IDMP) in Europe ; Chapter 2

Following the publication of version 1 in February 2020, the content of this document was amended to:
• Updated scope of this guidance
• Updated medicinal products in scope
• Updated content of submission of medicinal products using FHIR
• Updated structure and contents of identifier and defining characteristics of a medicinal product entry in PMS
• Updated Figure 1 and contents in user guidance
• Added provenance resource…