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 objectives of this Workshop are to present in some detail the history, and particularly the present organisational structure, data flows and technical details of the ePrecription/eDispensation and Patient Summary healthcare services as provided in the context of the CEF eHDSI and to give a preliminary glimpse of the new requirements resulting from IDMP implementation […]
The objectives of this Workshop are to present in some detail the history, and particularly the present organisational structure, data flows and technical details of the ePrecription/eDispensation and Patient Summary healthcare services as provided in the context of the CEF eHDSI and to give a preliminary glimpse of the new requirements resulting from IDMP implementation […]
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.
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 […]
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 […]
The current status of UNICOM work and expected results is presented by C.Hay (WP1) at the meeting of the International pharmaceutical regulators programme (http://www.iprp.global/home)
Preliminary Program Welcome – Agenda State of play with Vaccination Standards in Europe: an overview Christof Gessner, HL7 Europe Board of Directors, HL7 Germany What is the state of play of implementations across Europe? Role of HL7 Standards? Role of Affiliates? collaborations – decision-making practices – vendor engagement? Vaccination Standardization Efforts across Europe (deep dive, […]
UNICOM – EMA Implementation Guide v2.0 The course of IDMP implementation in Europe is strongly influenced by European Medicines Agency's (EMA) guidance. On Monday 22 February, EMA released version 2.0 of its Implementation guide (EU IG v2.0). This is a very important milestone for UNICOM and our communities, which will be presented and discussed at our […]
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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 […]
