Name: CEN ISO/TS 19256:2017
Brand: CEN

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

Published date

03-22-2017

Publisher

Comite Europeen de Normalisation

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

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.

Committee	CEN/TC 251
DocumentType	Technical Specification
PublisherName	Comite Europeen de Normalisation
Status	Current

Standards	Relationship
DIN CEN ISO/TS 19256;DIN SPEC 13236:2017-06	Identical
ISO/TS 19256:2016	Identical
UNI CEN ISO/TS 19256 : 2017	Identical
S.R. CEN ISO/TS 19256:2017	Identical
UNE-CEN ISO/TS 19256:2017	Identical
NEN NVN CEN ISO/TS 19256 : 2017	Identical
PD CEN ISO/TS 19256:2017	Identical
DIN CEN ISO/TS 19256 : 2017	Identical

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