Prototype ISO IDMP Compliant Datafeed to eHealth (Deliverable D4.12)
1.0.0 - STU1 International flag

Prototype ISO IDMP Compliant Datafeed to eHealth (Deliverable D4.12), published by UNICOM. This guide is not an authorized publication; it is the continuous build for version 1.0.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/unicom-project-eu/d4.12/ and changes regularly. See the Directory of published versions

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Official URL: http://unicom-project.eu/fhir/d4-12/ImplementationGuide/unicom.fhir.idmp-datafeed Version: 1.0.0
Draft as of 2023-07-22 Computable Name: D412

Introduction

This Implementation Guide is a prototype for providing ISO IDMP compliant medication data to eHealth and other national stakeholders.

The implementation guide is based on UNICOM Implementation Guide in its core data. However, the current deliverable goes beyond ISO IDMP, reflecting also the national level requirements that are common for many countries in Europe. This information is gathered from the NCAs as well as their national eHealth partners.

Specification

The specification aims to be a prototype, suitable for most NCAs for planning their public data feed after aligning their inner information systems with ISO IDMP. The specification is initially created as part of UNICOM Work Package 4 deliverable "D4.12 Prototype presentation of IDMP compatible datafeeds to eHealth consumers".

Content of the Implementation Guide:

  • Logical data model;
  • FHIR profiles for related resources;
  • Example data;
  • Guidance on which coded terminologies to use;
  • Background information about the rationale behind implementation choices.

Related resources:

Related UNICOM deliverables:

  • D5.1: Business requirements for the adoption of IDMP in eHealth Services
  • D5.2: Guidelines for IDMP-based Cross-Border ePrescription / eDispensation & Patient Summary
  • D5.7: Common minimum data set for implementation in the national NCA and eHealth solutions.
  • D9.1: An analysis of the IDMP medicinal product identification data provided by NCAs (and SPOR) compared to that needed in MPD for clinical care and for secondary uses.
  • D9.3: Report on the Specification(s) and delivery technology for IDMP data delivery from NCA to MPD.
  • D9.4: IDMP Implementation guidance for pharmacy system suppliers (focus on patient medication list) - Common minimum data set.

Contributors

Medicines agencies:

  • Belgium
  • Estonia
  • Portugal

Technical support

  • HL7 Belgium
  • HL7 Portugal