EN ISO 11240:2012
Current
The latest, up-to-date edition.
Health informatics - Identification of medicinal products - Data elements and structures for the unique identification and exchange of units of measurement (ISO 11240:2012)
01-11-2012
Foreword
Introduction
1 Scope
2 Normative references
3 Terms, definitions and abbreviated terms
4 Structures and vocabularies
Annex A (informative) - Using units of measurement
for expression of medicinal product strength
Annex B (informative) - Examples to describe data
elements
Annex C (informative) - Example - Controlled
terminology mapping
Annex D (informative) - Domain analysis model
Bibliography
ISO 11240:2012:specifies rules for the usage and coded representation of units of measurement for the purpose of exchanging information about quantitative medicinal product characteristics that require units of measurement (e.g. strength) in the human medicine domain;establishes requirements for units in order to provide traceability to international metrological standards;provides rules for the standardized and machine-readable documentation of quantitative composition and strength of medicinal products, specifically in the context of medicinal product identification;defines the requirements for the representation of units of measurement in coded form;provides structures and rules for mapping between different unit vocabularies and language translations to support the implementation of ISO 11240:2012, taking into account that existing systems, dictionaries and repositories use a variety of terms and codes for the representation of units.The scope of ISO 11240:2012 is limited to the representation of units of measurement for data interchange between computer applications.
Committee |
CEN/TC 251
|
DocumentType |
Standard
|
PublisherName |
Comite Europeen de Normalisation
|
Status |
Current
|
Standards | Relationship |
I.S. EN ISO 11240:2012 | Identical |
PN EN ISO 11240 : 2013 | Identical |
SN EN ISO 11240:2013 | Identical |
UNE-EN ISO 11240:2013 | Identical |
NEN EN ISO 11240 : 2012 | Identical |
BS EN ISO 11240:2012 | Identical |
DIN EN ISO 11240:2013-03 | Identical |
NF EN ISO 11240 : 2013 | Identical |
UNI EN ISO 11240 : 2012 | Identical |
NBN EN ISO 11240 : 2013 | Identical |
NS EN ISO 11240 : 2012 | Identical |
ISO 11240:2012 | Identical |
ISO 1087-1:2000 | Terminology work Vocabulary Part 1: Theory and application |
EN 1614:2006 | Health informatics - Representation of dedicated kinds of property in laboratory medicine |
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/IEC 9834-1:2012 | Information technology — Procedures for the operation of object identifier registration authorities — Part 1: General procedures and top arcs of the international object identifier tree |
ISO/HL7 27953-2:2011 | Health informatics — Individual case safety reports (ICSRs) in pharmacovigilance — Part 2: Human pharmaceutical reporting requirements for ICSR |
ISO/HL7 27951:2009 | Health informatics Common terminology services, release 1 |
ISO 21090:2011 | Health informatics — Harmonized data types for information interchange |
ISO/IEC Guide 99:2007 | International vocabulary of metrology Basic and general concepts and associated terms (VIM) |
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 |
ISO 9000:2015 | Quality management systems — Fundamentals and vocabulary |
ISO/HL7 27953-1:2011 | Health informatics — Individual case safety reports (ICSRs) in pharmacovigilance — Part 1: Framework for adverse event reporting |
EN 14463:2007 | Health informatics - A syntax to represent the content of medical classification systems - ClaML |
EN 12435:2006 | Health informatics - Expression of results of measurements in health sciences |
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 |
Access your standards online with a subscription
Features
-
Simple online access to standards, technical information and regulations.
-
Critical updates of standards and customisable alerts and notifications.
-
Multi-user online standards collection: secure, flexible and cost effective.