Guide to the International Standards for Identification of Medicinal Products (IDMP)

For many of those who work within Regulatory Operations, support IT departments, and particularly those involved in Regulatory Information Management (RIM) systems and the eXtended Eudravigilance Medicinal Product Dictionary (XEVMPD), the term ‘IDMP’ is being talked about a lot and increasingly so. For those who are not talking about it yet, you will be soon. This guide aims to inform regulatory stakeholders why IDMP is important, and answers these key questions:

• Why are the standards needed?
• What do the standards cover?
• How can I best prepare my organization for implementation?
• What are the global implementation plans?

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