The UNICOM project has compiled and published a set of requirements for a new Identification of Medicinal Products (IDMP) logical model, which will be technology independent.
During this interactive session the presenters will share with you the content and creation process of the work. Together with the panellists, the role of an IDMP logical model will be discussed, and how this document can contribute to its development by International Organization for Standardization (ISO)/TC 215 Health Informatics WG6.
Currently, the IDMP data model is described in two ways: by partial logical models across the different standards making up the IDMP set of standards, and by High Level Seven (HL7) v3 based specifications in some of the technical specifications.
The ISO group of experts will take these requirements as input for the development of a new ISO IDMP logical model. The discussion of the requirements will also be made available to the ISO experts, as they will join the conversation.