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14/30267009 DC : 0

Superseded

Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

View Superseded by

BS EN ISO 17523 - HEALTH INFORMATICS - REQUIREMENTS FOR ELECTRONIC PRESCRIPTIONS

Available format(s)

Hardcopy , PDF

Superseded date

31-07-2016

Superseded by

BS EN ISO 17523:2016

Language(s)

English

€23.37
Excluding VAT

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

BS EN ISO 17523.

Committee
IST/35
DocumentType
Draft
Pages
24
PublisherName
British Standards Institution
Status
Superseded
SupersededBy

NEN 7503 : 2011 HEALTH INFORMATICS - MESSAGES - ELECTRONIC EXCHANGE OF MESSAGES WITH PRESCRIPTIONS AND DISPENSATIONS
ISO/TS 27527:2010 Health informatics Provider identification
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 21549-7:2016 Health informatics — Patient healthcard data — Part 7: Medication data
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
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/TR 22790:2007 Health informatics Functional characteristics of prescriber support systems
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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