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  • CEN ISO/TS 19256:2017

    Current The latest, up-to-date edition.

    Health informatics - Requirements for medicinal product dictionary systems for health care (ISO/TS 19256:2016)

    Available format(s): 

    Language(s): 

    Published date:  22-03-2017

    Publisher:  Comite Europeen de Normalisation

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

    European foreword
    Foreword
    Introduction
    1 Scope
    2 Normative references
    3 Terms and definitions
    4 Abbreviated terms
    5 Boundary between MPD-systems and IDMP, ancillary
      information to build an MPD-system and local implementation
    6 Positioning of Medicinal Product Dictionary Systems
      for Healthcare
    7 The Functional Requirements for MPD-systems
    Annex A (informative) - IDMP series in context, serving
            this Technical Specification
    Bibliography

    Abstract - (Show below) - (Hide below)

    ISO/TS 19256:2016 defines the required characteristics for any MPD-system to support use cases in healthcare.These characteristics include the medication concepts, identifiers and relationships to form a kind of structure that supports the use cases.

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

    Committee CEN/TC 251
    Document Type Technical Specification
    Publisher Comite Europeen de Normalisation
    Status Current

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

    ISO 18308:2011 Health informatics — Requirements for an electronic health record architecture
    CEN/TS 15699:2009 Health informatics - Clinical knowledge resources - Metadata
    ISO 1087-1:2000 Terminology work Vocabulary Part 1: Theory and application
    ISO 13119:2012 Health informatics — Clinical knowledge resources — Metadata
    ISO 13940:2015 Health informatics — System of concepts to support continuity of care
    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/HL7 27953-2:2011 Health informatics — Individual case safety reports (ICSRs) in pharmacovigilance — Part 2: Human pharmaceutical reporting requirements for ICSR
    ISO 21549-7:2016 Health informatics — Patient healthcard data — Part 7: Medication data
    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
    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
    ISO 19115-1:2014 Geographic information — Metadata — Part 1: Fundamentals
    ISO 17523:2016 Health informatics — Requirements for electronic prescriptions
    ISO/HL7 10781:2015 Health Informatics — HL7 Electronic Health Records-System Functional Model, Release 2 (EHR FM)
    ISO 704:2009 Terminology work — Principles and methods
    ISO/TS 17439:2014 Health informatics Development of terms and definitions for health informatics glossaries
    ISO 11239:2012 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
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