Health Informatics - Business requirements for a syntax to exchange structured dose information for medicinal products (ISO/TS 17251:2016)

ISO/TS 17251:2016 specifies the business requirements for the structured content of structured or semi-structured dose instructions for recording dose instructions in the electronic health record (EHR), supporting clinical decision support, and in exchanging medication orders, as applicable to primary, secondary and tertiary care.
NOTE          See 2.9, note to entry, regarding the use of "medication order" and "prescription".
Comprehension of dose instructions by the patient is an overarching consideration for patient safety and the best patient outcomes. Related factors are discussed, but are not part of the primary scope.
It does not define an information model, except to the extent that those information model concepts are necessary to define business requirements.
Outside the scope of ISO/TS 17251:2016 are:
-      the functionality of health, clinical and/or pharmacy systems;
-      other kinds of content of health, clinical or pharmacy systems that are needed to support the whole process of health care providers, such as:
-      wide range of knowledge about medicines that would be handled in drug knowledge databases and decision support systems;
-      the complete medical record (EHR);
-      a medicinal product dictionary.

Medizinische Informatik - Geschäftsanforderungen an eine Syntax zum Austausch von Dosisinformationen für Arzneimittel (ISO/TS 17251:2016)

Informatique de santé - Exigences d'affaire pour une syntaxe d'échange d'informations de dose structurée pour les produits médicaux (ISO/TS 17251:2016)

Zdravstvena informatika - Poslovne zahteve za sintakso za izmenjavo strukturiranih podatkov odmerkov za zdravila (ISO/TS 17251:2016)

ISO/TS 17251:2016 določa poslovne zahteve za strukturirano vsebino strukturiranih ali polstrukturiranih navodil za odmerke za shranjevanje navodil za odmerke v elektronski zdravstveni zapis (EHR), zagotavljanje podpore za klinično odločanje ter uporabo v izmenjavi naročil zdravil, kot se uporabljajo v primarni, sekundarni in terciarni oskrbi.
OPOMBA: Glej točko 2.9, opomba k izrazu, v zvezi z uporabo izrazov »naročilo zdravila« in »recept«.
Bolnikovo razumevanje navodil za odmerke je najpomembnejši vidik za zagotavljanje njegove varnosti in najboljših rezultatov zdravljenja. Obravnavani so povezani dejavniki, ki pa niso del primarnega področja uporabe.
Standard ne določa informacijskega modela, razen v obsegu, v katerem so ti koncepti informacijskega modela potrebni za opredelitev poslovnih zahtev.
Naslednji vidiki ne spadajo na področje uporabe standarda:ISO/TS 17251:2016:
– funkcionalnost zdravstvenih, kliničnih in/ali lekarniških sistemov;
– druge vrste vsebin zdravstvenih, kliničnih ali lekarniških sistemov, ki so potrebne za zagotavljanje podpore za celoten postopek ponudnikov zdravstvenih storitev, kot so:
– širok obseg znanja o zdravilih, vključenih v podatkovnih zbirkah znanja o zdravilih in sistemih za zagotavljanje podpore za sprejemanje odločitev;
– celovit elektronski zdravstveni zapis;
– slovar zdravil.

General Information

Status
Withdrawn
Publication Date
19-Jul-2016
Withdrawal Date
14-Mar-2023
Current Stage

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Standards Content (Sample)

SLOVENSKI STANDARD
SIST-TS CEN ISO/TS 17251:2017
01-februar-2017
Zdravstvena informatika - Poslovne zahteve za sintakso za izmenjavo
strukturiranih podatkov odmerkov za zdravila (ISO/TS 17251:2016)
Health Informatics - Business requirements for a syntax to exchange structured dose
information for medicinal products (ISO/TS 17251:2016)
Medizinische Informatik - Geschäftsanforderungen an eine Syntax zum Austausch von
Dosisinformationen für Arzneimittel (ISO/TS 17251:2016)
Informatique de santé - Exigences d'affaire pour une syntaxe d'échange d'informations
de dose structurée pour les produits médicaux (ISO/TS 17251:2016)
Ta slovenski standard je istoveten z: CEN ISO/TS 17251:2016
ICS:
11.120.10 Zdravila Medicaments
35.240.80 Uporabniške rešitve IT v IT applications in health care
zdravstveni tehniki technology
SIST-TS CEN ISO/TS 17251:2017 en,fr,de
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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SIST-TS CEN ISO/TS 17251:2017

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SIST-TS CEN ISO/TS 17251:2017


CEN ISO/TS 17251
TECHNICAL SPECIFICATION

SPÉCIFICATION TECHNIQUE

July 2016
TECHNISCHE SPEZIFIKATION
ICS 35.240.80
English Version

Health Informatics - Business requirements for a syntax to
exchange structured dose information for medicinal
products (ISO/TS 17251:2016)
Informatique de santé - Exigences d'affaire pour une Medizinische Informatik - Geschäftsanforderungen an
syntaxe d'échange d'informations de dose structurée eine Syntax zum Austausch von Dosisinformationen für
pour les produits médicaux (ISO/TS 17251:2016) Arzneimittel (ISO/TS 17251:2016)
This Technical Specification (CEN/TS) was approved by CEN on 10 July 2016 for provisional application.

The period of validity of this CEN/TS is limited initially to three years. After two years the members of CEN will be requested to
submit their comments, particularly on the question whether the CEN/TS can be converted into a European Standard.

CEN members are required to announce the existence of this CEN/TS in the same way as for an EN and to make the CEN/TS
available promptly at national level in an appropriate form. It is permissible to keep conflicting national standards in force (in
parallel to the CEN/TS) until the final decision about the possible conversion of the CEN/TS into an EN is reached.

CEN members are the national standards bodies of Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia,
Finland, Former Yugoslav Republic of Macedonia, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania,
Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and
United Kingdom.





EUROPEAN COMMITTEE FOR STANDARDIZATION
COMITÉ EUROPÉEN DE NORMALISATION

EUROPÄISCHES KOMITEE FÜR NORMUNG

CEN-CENELEC Management Centre: Avenue Marnix 17, B-1000 Brussels
© 2016 CEN All rights of exploitation in any form and by any means reserved Ref. No. CEN ISO/TS 17251:2016 E
worldwide for CEN national Members.

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SIST-TS CEN ISO/TS 17251:2017
CEN ISO/TS 17251:2016 (E)
Contents Page
European Foreword . 3

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SIST-TS CEN ISO/TS 17251:2017
CEN ISO/TS 17251:2016 (E)
European Foreword
This document (CEN ISO/TS 17251:2016) has been prepared by Technical Committee ISO/TC 215
“Health informatics” in collaboration with Technical Committee CEN/TC 251 “Health informatics” the
secretariat of which is held by NEN.
Attention is drawn to the possibility that some of the elements of this document may be the subject of
patent rights. CEN [and/or CENELEC] shall not be held responsible for identifying any or all such patent
rights.
According to the CEN-CENELEC Internal Regulations, the national standards organizations of the
following countries are bound to announce this Technical Specification: Austria, Belgium, Bulgaria,
Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, Former Yugoslav Republic of Macedonia,
France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta,
Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland,
Turkey and the United Kingdom.
Endorsement notice
The text of ISO/TS 17251:2016 has been approved by CEN as CEN ISO/TS 17251:2016 without any
modification.
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SIST-TS CEN ISO/TS 17251:2017

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SIST-TS CEN ISO/TS 17251:2017
TECHNICAL ISO/TS
SPECIFICATION 17251
First edition
2016-07-01
Health inf
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