BS EN ISO 11239:2012
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
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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
Hardcopy , PDF
16-06-2023
English
30-11-2012
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Foreword
Introduction
1 Scope
2 Normative references
3 Terms, definitions and abbreviations
4 Requirements
5 Schema
Annex A (informative) - Examples of controlled
vocabularies
Annex B (informative) - Examples of controlled
vocabularies to describe medicinal products
Bibliography
Describes: - the data elements, structures and relationships between the data elements required for the exchange of information, which uniquely and with certainty identify pharmaceutical dose forms, units of presentation, routes of administration and packaging items (containers, closures and administration devices) related to medicinal products; - a mechanism for the association of translations of a single concept into different languages, which is an integral part of the information exchange; - a mechanism for the versioning of the concepts in order to track their evolution; - rules to allow regional authorities to map existing regional terms to the terms created using this International Standard, in a harmonized and meaningful way.
| Committee |
IST/35
|
| DevelopmentNote |
Supersedes 10/30229861 DC. (11/2012)
|
| DocumentType |
Standard
|
| Pages |
40
|
| PublisherName |
British Standards Institution
|
| Status |
Superseded
|
| SupersededBy | |
| Supersedes |
This International Standard specifies:
-
the data elements, structures and relationships between the data elements required for the exchange of information, which uniquely and with certainty identify pharmaceutical dose forms, units of presentation, routes of administration and packaging items (containers, closures and administration devices) related to medicinal products;
-
a mechanism for the association of translations of a single concept into different languages, which is an integral part of the information exchange;
-
a mechanism for the versioning of the concepts in order to track their evolution;
-
rules to allow regional authorities to map existing regional terms to the terms created using this International Standard, in a harmonized and meaningful way.
In addition, to support the successful application of this International Standard, references to standards concerned with identification of medicinal products (IDMP) and messaging for medicinal product information are provided as required.
| Standards | Relationship |
| ISO 11239:2012 | Identical |
| EN ISO 11239:2012 | Identical |
| 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 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 |
| ENV 13607:2000 | Health informatics - Messages for the exchange of information on medicine prescriptions |
| 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 |
| ENV 12610:1997 | Medical informatics - Medicinal product identification |
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