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)
22-03-2017
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 |
| PNE-FprCEN ISO/TS 19256 | 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 |
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