The definition of an ‘IDMP Medicinal Product’ can be complex and putting together information about medicinal products in the ISO IDMP data model can be quite a challenge if an organization doesn’t understand the intricacies of the data model and the levels of the product at which unique identifiers are assigned.
Until this is done, any effort on IDMP data-gathering and cleansing will only lead to future re-work when IDMP submissions are rejected, as the submitted HL7 file won’t comply with the guidelines.
This paper discusses how the ISO IDMP model can be used to describe various types of medicinal products.
The paper also explains the Medicinal Product Identifier, Packaged Medicinal Product Identifier and Batch Identifiers, and how these identifiers can be impacted by various factors.
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