External events related to UNICOM

How digitalisation can support the regulatory business process ​Britt Vermeij, Vice-Chair of the Regulatory and Scientific Affairs Committee Medicines for Europe, TEVA - A coherent data strategy as foundation to respond to public health needs Remco Munnik, Chair of the Telematics WG Medicines for Europe, Iperion - Open dialogue between industry and regulators: How digitalisation […]

​UNICOM – Pharmaceutical Dose Forms The presenters will share their perspective on how the pharmaceutical dose forms have been developed and are currently used in different situations. They will give insight in the current revision of the ISO standard, which intends to provide easier means to define world wide unique pharmaceutical dose forms.

The UNICOM project has compiled and published a set of requirements for a new IDMP logical model, which shall be technology independent. Currently, the IDMP data model is described by partial logical models across the different standards making up the IDMP set of standards and by 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. Our discussion of the requirements will also be made available to the ISO experts, as they join the conversation.​

Transcending national boundaries and organizations, the Joint Initiative Council’s standards development organizations work collaboratively to provide global, coordinated—not competitive—standards that address real-world healthcare issues. In its recently released white paper, the JIC explores the desired future of a digital health ecosystem where high-quality data is available to the right people, at the right place and […]