This page is part of the Electronic Medicinal Product Information (ePI) FHIR Implementation Guide (v1.0.0-ballot: STU1 Ballot 1) based on FHIR v5.0.0-ballot. . For a full list of available versions, see the Directory of published versions
Appendix
Glossary
To be added at a later time.
Copyrights
This guide, as well the artifacts developed by HL7® including terminologies, is produced by HL7 under the terms of HL7® Governance and Operations Manual relating to Intellectual Property (Section 16), specifically its copyright, trademark and patent provisions.
This document is licensed under Creative Commons “No Rights Reserved” (CCO).
HL7®, HEALTH LEVEL SEVEN®, FHIR® and the FHIR ® are trademarks owned by Health Level Seven International, registered with the United States Patent and Trademark Office.
This HL7 specification contains and references intellectual property owned by third parties (“Third Party IP”).
Implementers and testers of this specification SHALL abide by the license requirements for each terminology content artifact utilized within a functioning implementation. Terminology licenses SHALL be obtained from the Third Party IP owner for each code system and/or other specified artifact used. It is the sole responsibility of each organization deploying or testing this specification to ensure their implementations comply with licensing requirements of each Third Party IP.
Following is a non-exhaustive list of third-party terminologies used in this guide that may require a separate license:
Terminology |
Owner/Contact |
Links |
EDQM Standard Terms |
European Directorate for the Quality of Medicines (EDQM) |
https://www.edqm.eu/en/standard-terms-database |
ISO 3166 Country Code |
International Organization for Standardization (ISO) |
https://www.iso.org/iso-3166-country-codes.html |
ISO 639-1 Language Code |
International Organization for Standardization (ISO) |
https://www.iso.org/iso-639-language-codes.html |
Unified Codes for Units of Measures (UCUM) |
Regenstrief Institute, Inc. and the UCUM Organization |
http://unitsofmeasure.org/trac/wiki/TermsOfUse |
References
- There are no sources in the current document.
- FHIR Validation - https://www.hl7.org/fhir/validation.html
- FHIR Narrative specification - http://hl7.org/fhir/5.0.0-snapshot1/narrative.html#Narrative
- FHIR Document specification - https://build.fhir.org/documents.html
- Web Content Accessibility Guidelines (WCAG) international standard - https://www.w3.org/TR/WCAG21/
- International Patient Summary Implementation Guide
- EMA - Electronic Product Information (ePI) Standard and API Specification v1 (Document version 1.2)
- ISO 639-1, Codes for the representation of names of languages — Part 1: Alpha-2 code
- ISO 3166-1:2013, Codes for the representation of names of countries and their subdivisions — Part 1: Country codes
- ISO 8601, Data elements and interchange formats — Information interchange — Representation of dates and times
- ISO 11238, Health informatics — Identification of Medicinal Products — Data elements and structures for the unique identification and exchange of regulated information on substances
- ISO 11239, Health informatics — Identification of Medicinal Products — Data elements and structures for the unique identification and exchange of regulated information on pharmaceutical dose forms, units of presentation, routes of administration and packaging
- ISO 11240, Health informatics — Identification of Medicinal Products — Data elements and structures for the unique identification and exchange of units of measurement
- ISO 11616, Health informatics — Identification of Medicinal Products — Data elements and structures for the unique identification and exchange of regulated pharmaceutical product information
- ISO/TS 19844, Health informatics — Identification of Medicinal Products — Implementation guidelines for data elements and structures for the unique identification and exchange of regulated information on substances
- ISO/TS 20440, Health informatics — Identification of Medicinal Products — Implementation guide for ISO 11239 data elements and structures for the unique identification and exchange of regulated information on pharmaceutical dose forms, units of presentation, routes of administration and packaging
- ISO/TS 20443, Health informatics — Identification of Medicinal Products — Implementation guide for ISO 11615 data elements and structures for the unique identification and exchange of regulated Medicinal Product information
- ISO/TS 20451, Health informatics — Identification of Medicinal Products — Implementation guide for ISO 11616 data elements and structures for the unique identification and exchange of regulated pharmaceutical product information