• BS EN ISO 11239:2012

    Superseded A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

    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

    Available format(s):  Hardcopy, PDF

    Superseded date:  16-06-2023

    Language(s):  English

    Published date:  30-11-2012

    Publisher:  British Standards Institution

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    Table of Contents - (Show below) - (Hide below)

    Foreword
    Introduction
    1 Scope
    2 Normative references
    3 Terms, definitions and abbreviations
    4 Requirements
    5 Schema
    Annex A (informative) - Examples of controlled
            vocabularies
    Annex B (informative) - Examples of controlled
            vocabularies to describe medicinal products
    Bibliography

    Abstract - (Show below) - (Hide below)

    Describes: - the data elements, structures and relationships between the data elements required for the exchange of information, which uniquely and with certainty identify pharmaceutical dose forms, units of presentation, routes of administration and packaging items (containers, closures and administration devices) related to medicinal products; - a mechanism for the association of translations of a single concept into different languages, which is an integral part of the information exchange; - a mechanism for the versioning of the concepts in order to track their evolution; - rules to allow regional authorities to map existing regional terms to the terms created using this International Standard, in a harmonized and meaningful way.

    Scope - (Show below) - (Hide below)

    This International Standard specifies:

    • the data elements, structures and relationships between the data elements required for the exchange of information, which uniquely and with certainty identify pharmaceutical dose forms, units of presentation, routes of administration and packaging items (containers, closures and administration devices) related to medicinal products;

    • a mechanism for the association of translations of a single concept into different languages, which is an integral part of the information exchange;

    • a mechanism for the versioning of the concepts in order to track their evolution;

    • rules to allow regional authorities to map existing regional terms to the terms created using this International Standard, in a harmonized and meaningful way.

    In addition, to support the successful application of this International Standard, references to standards concerned with identification of medicinal products (IDMP) and messaging for medicinal product information are provided as required.

    General Product Information - (Show below) - (Hide below)

    Committee IST/35
    Development Note Supersedes 10/30229861 DC. (11/2012)
    Document Type Standard
    Publisher British Standards Institution
    Status Superseded
    Superseded By
    Supersedes

    Standards Referencing This Book - (Show below) - (Hide below)

    ISO 11615:2017 Health informatics — Identification of medicinal products — Data elements and structures for the unique identification and exchange of regulated medicinal product information
    ISO 21090:2011 Health informatics — Harmonized data types for information interchange
    ISO 11240:2012 Health informatics Identification of medicinal products Data elements and structures for the unique identification and exchange of units of measurement
    ENV 13607:2000 HEALTH INFORMATICS - MESSAGES FOR THE EXCHANGE OF INFORMATION ON MEDICINE PRESCRIPTIONS
    ISO 11238:2012 Health informatics Identification of medicinal products Data elements and structures for the unique identification and exchange of regulated information on substances
    ISO 11616:2017 Health informatics — Identification of medicinal products — Data elements and structures for unique identification and exchange of regulated pharmaceutical product information
    ENV 12610 : DRAFT 1997 MEDICAL INFORMATICS - MEDICINAL PRODUCT IDENTIFICATION
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