14/30267009 DC : 0
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
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BS EN ISO 17523 - HEALTH INFORMATICS - REQUIREMENTS FOR ELECTRONIC PRESCRIPTIONS
Hardcopy , PDF
English
31-07-2016
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Superseded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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