Description: Referring to the landscape of medicinal product data – from “research and development” to “utilisation and outcome assessments”- the vision is that the essential IDMP identifiers remain used and unchanged along that life cycle. This Community of Expertise (CoE) will provide opportunity : for industry to present their perspective and needs, with large international […]
The 4th of November a Community of Expertise will be held for which you have been invited. The presenters will be Annet Rozema, Mirjam Keulen & Marcel Hoefnagel from CBG, The Netherlands, UNICOM WP 2. Substances have been the topic of the UNICOM Community of Expertise before and this is not a surprise as substances […]
UNICOM – Cross-border ePrescription - standards, terminologies, processes You will learn what UNICOM is expected to contribute in order to make this service truly operational and reliable: The implementation of IDMP across Europe provides important opportunities for the improvement of cross-border services, such as ePrescription. UNICOM is tasked with elaborating these opportunities into change proposals […]
The importance of medicinal product dictionaries (MPDs) is highlighted by two concrete examples. MPDs bring together the information on medicinal products from NCA and a variety of sources. Making sure that the identification of the medicinal product across these sources can be done automatically and without error, makes the implementation of IDMP such a crucial […]
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 […]
Joint Initiative Council Open Forum - Morning Session 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 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.
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 Innovation Action has received funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement No. 875299.
