Health informatics - Identification of medicinal products - Data elements and structures for the unique identification and exchange of regulated medicinal product information - Amendment 1 (ISO 11615:2017/Amd 1:2022)

Medizinische Informatik - Identifikation von Arzneimitteln - Datenelemente und Strukturen zur eindeutigen Identifikation und zum Austausch von vorgeschriebenen Arzneimittelinformationen - Änderung 1 (ISO 11615:2017/Amd 1:2022)

No scope available

Informatique de santé - Identification des médicaments - Éléments de données et structures pour l'identification unique et l'échange d'informations sur les médicaments contrôlés - Amendement 1 (ISO 11615:2017/Amd 1:2022)

Zdravstvena informatika - Identifikacija zdravil - Elementi in zgradba podatkov za enotno identifikacijo in izmenjavo predpisanih informacij o zdravilih - Dopolnilo A1 (ISO 11615:2017/Amd 1:2022)

General Information

Status
Published
Publication Date
20-Sep-2022
Current Stage
6060 - Definitive text made available (DAV) - Publishing
Start Date
21-Sep-2022
Completion Date
21-Sep-2022

Relations

Effective Date
03-Jun-2020
Effective Date
06-Dec-2023

Overview

EN ISO 11615:2017/A1:2022 - Health informatics - Identification of medicinal products - Data elements and structures for the unique identification and exchange of regulated medicinal product information (Amendment 1) is a CEN-endorsed amendment to ISO 11615:2017. Approved by CEN on 12 August 2022 and endorsed for national adoption by March 2023, this document supports consistent, machine-readable representation of regulated medicinal product information across regulatory, clinical and healthcare systems.

Key topics and technical updates

  • Scope: defines data elements and data structures used for the unique identification and exchange of regulated medicinal product information (IDMP).
  • Amendment highlights:
    • Revision to the Introduction to reference other normative IDMP and messaging standards to support successful information exchange.
    • Addition to clause 7.5.4 pointing implementers to new translation/synonym resources.
    • New informative Annex C providing language translations and synonyms for class names and attributes used in the IDMP data model (complements Annexes A and B).
  • Content emphasis:
    • Consistent semantic definitions for class names, attributes and data elements in the IDMP model.
    • Implementation considerations for regional/local language translations and synonym usage to ensure semantic interoperability.
  • Maintenance and provenance:
    • Prepared by ISO/TC 215 (Health informatics) in collaboration with CEN/TC 251; text adopted unchanged by CEN as EN ISO 11615:2017/A1:2022.
    • Annex C translations and full lists are available via the ISO Standards Maintenance Portal: https://standards.iso.org/iso/11615/ed-2/en/amd/1

Practical applications

  • Improves interoperability of medicinal product data across:
    • National medicines agencies and regulatory submissions
    • Pharmacovigilance and safety reporting systems
    • Clinical information systems, e‑prescribing and pharmacy IT
    • Healthcare data exchanges and public health reporting
  • Helps implementers map local terminology and multilingual labels to standard IDMP concepts, reducing ambiguity in cross-border data exchange and regulatory workflows.

Who should use this standard

  • Regulatory authorities and national competent authorities
  • Pharmaceutical companies (regulatory affairs, data management)
  • Health informatics vendors, EHR and e-prescribing system developers
  • Pharmacovigilance and safety surveillance teams
  • Hospitals, health insurers and governmental health IT programs seeking consistent medicinal product identification

Related standards and keywords

  • Related: ISO 11615 family (IDMP), IDMP messaging standards referenced in the amendment
  • SEO keywords: EN ISO 11615:2017/A1:2022, IDMP, identification of medicinal products, data elements, medicinal product information, health informatics, interoperability, pharmacovigilance, regulatory exchange, translations and synonyms
Amendment

EN ISO 11615:2018/A1:2023

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Frequently Asked Questions

EN ISO 11615:2017/A1:2022 is a amendment published by the European Committee for Standardization (CEN). Its full title is "Health informatics - Identification of medicinal products - Data elements and structures for the unique identification and exchange of regulated medicinal product information - Amendment 1 (ISO 11615:2017/Amd 1:2022)". This standard covers: No scope available

No scope available

EN ISO 11615:2017/A1:2022 is classified under the following ICS (International Classification for Standards) categories: 35.240.80 - IT applications in health care technology. The ICS classification helps identify the subject area and facilitates finding related standards.

EN ISO 11615:2017/A1:2022 has the following relationships with other standards: It is inter standard links to EN ISO 11615:2017, prEN ISO 11615. Understanding these relationships helps ensure you are using the most current and applicable version of the standard.

EN ISO 11615:2017/A1:2022 is available in PDF format for immediate download after purchase. The document can be added to your cart and obtained through the secure checkout process. Digital delivery ensures instant access to the complete standard document.

Standards Content (Sample)


SLOVENSKI STANDARD
01-januar-2023
Zdravstvena informatika - Identifikacija zdravil - Elementi in zgradba podatkov za
enotno identifikacijo in izmenjavo predpisanih informacij o zdravilih - Dopolnilo A1
(ISO 11615:2017/Amd 1:2022)
Health informatics - Identification of medicinal products - Data elements and structures
for the unique identification and exchange of regulated medicinal product information -
Amendment 1 (ISO 11615:2017/Amd 1:2022)
Medizinische Informatik - Identifikation von Arzneimitteln - Datenelemente und Strukturen
zur eindeutigen Identifikation und zum Austausch von vorgeschriebenen
Arzneimittelinformationen - Änderung 1 (ISO 11615:2017/Amd 1:2022)
Informatique de santé - Identification des médicaments - Éléments de données et
structures pour l'identification unique et l'échange d'informations sur les médicaments
contrôlés - Amendement 1 (ISO 11615:2017/Amd 1:2022)
Ta slovenski standard je istoveten z: EN ISO 11615:2017/A1:2022
ICS:
11.120.10 Zdravila Medicaments
35.240.80 Uporabniške rešitve IT v IT applications in health care
zdravstveni tehniki technology
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

EN ISO 11615:2017/A1
EUROPEAN STANDARD
NORME EUROPÉENNE
September 2022
EUROPÄISCHE NORM
ICS 35.240.80
English Version
Health informatics - Identification of medicinal products -
Data elements and structures for the unique identification
and exchange of regulated medicinal product information -
Amendment 1 (ISO 11615:2017/Amd 1:2022)
Informatique de santé - Identification des médicaments Medizinische Informatik - Identifikation von
- Éléments de données et structures pour Arzneimitteln - Datenelemente und Strukturen zur
l'identification unique et l'échange d'informations sur eindeutigen Identifikation und zum Austausch von
les médicaments contrôlés - Amendement 1 (ISO vorgeschriebenen Arzneimittelinformationen -
11615:2017/Amd 1:2022) Änderung 1 (ISO 11615:2017/Amd 1:2022)
This amendment A1 modifies the European Standard EN ISO 11615:2017; it was approved by CEN on 12 August 2022.

CEN members are bound to comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for inclusion of
this amendment into the relevant national standard without any alteration. Up-to-date lists and bibliographical references
concerning such national standards may be obtained on application to the CEN-CENELEC Management Centre or to any CEN
member.
This amendment exists in three official versions (English, French, German). A version in any other language made by translation
under the responsibility of a CEN member into its own language and notified to the CEN-CENELEC Management Centre has the
same status as the official versions.

CEN members are the national standards bodies of Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia,
Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway,
Poland, Portugal, Republic of North Macedonia, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, Türkiye and
United Kingdom.
EUROPEAN COMMITTEE FOR STANDARDIZATION
COMITÉ EUROPÉEN DE NORMALISATION

EUROPÄISCHES KOMITEE FÜR NORMUNG

CEN-CENELEC Management Centre: Rue de la Science 23, B-1040 Brussels
© 2022 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 11615:2017/A1:2022 E
worldwide for CEN national Members.

Contents Page
European foreword . 3

European foreword
This document (EN ISO 11615:2017/A1:2022) has been prepared by Technical Committee ISO/TC 215
"Health informatics" in collaboration with Technical Committee CEN/TC 251 “Health informatics” the
secretariat of which is held by NEN.
This Amendment to the European Standard EN ISO 11615:2017 shall be given the status of a national
standard, either by publication of an identical text or by endorsement, at the latest by March 2023, and
conflicting national standards shall be withdrawn at the latest by March 2023.
Attention is drawn to the possibility that some of the elements of this document may be the subject of
patent rights. CEN shall not be held responsible for identifying any or all such patent rights.
Any feedback and questions on this document should be directed to the users’ national standards
body/national committee. A complete listing of these bodies can be found on the CEN website.
According to the CEN-CENELEC Internal Regulations, the national standards organizations of the
following countries are bound to implement this European Standard: Austria, Belgium, Bulgaria,
Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Iceland,
Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Republic of
North Macedonia, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, Türkiye and the
United Kingdom.
Endorsement notice
The text of ISO 11615:2017/Amd 1:2022 has been approved by CEN as EN ISO 11615:2017/A1:2022
without any modification.
INTERNATIONAL ISO
STANDARD 11615
Second edition
2017-10
AMENDMENT 1
2022-08
Health informatics — Identification
of medicinal products — Data
elements and structures for the
unique identification and exchange
of regulated medicinal product
information
AMENDMENT 1
Informatique de santé — Identification des médicaments — Éléments
de données et structures pour l'identification unique et l'échange
d'informations sur les médicaments contrôlés
AMENDEMENT 1
Reference number
ISO 11615:2017/Amd.1:2022(E)
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