Name: BS EN ISO 17523:2016
Brand: BSI

Health informatics. Requirements for electronic prescriptions

Published date

07-31-2016

Publisher

British Standards Institution

Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Conformance
5 General information
6 Requirements for electronic prescriptions
Annex A (normative) - Data elements
Annex B (informative) - Examples of elements and
implementations of electronic prescription
Bibliography

Describes a list of data elements that can be considered as essential for electronic prescriptions, depending on jurisdiction or clinical setting (primary healthcare, hospital, etc.).

Committee	IST/35
DevelopmentNote	Supersedes 14/30267009 DC. (07/2016)
DocumentType	Standard
PublisherName	British Standards Institution
Status	Current
Supersedes	14/30267009 DC : 0

Standards	Relationship
ISO 17523:2016	Identical
EN ISO 17523:2016	Identical

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ISO/IEC 24760-1:2011	Information technology Security techniques A framework for identity management Part 1: Terminology and concepts
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ISO/TS 22220:2011	Health informatics — Identification of subjects of health care
ISO 11240:2012	Health informatics Identification of medicinal products Data elements and structures for the unique identification and exchange of units of measurement
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ISO 11238:2012	Health informatics Identification of medicinal products Data elements and structures for the unique identification and exchange of regulated information on substances
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ISO 11616:2017	Health informatics — Identification of medicinal products — Data elements and structures for unique identification and exchange of regulated pharmaceutical product information
ISO 639-3:2007	Codes for the representation of names of languages — Part 3: Alpha-3 code for comprehensive coverage of languages
ISO 639-2:1998	Codes for the representation of names of languages — Part 2: Alpha-3 code
ISO/IEC 2382:2015	Information technology — Vocabulary
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