I.S. EN ISO 11238:2012
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
View Superseded by
HEALTH INFORMATICS - IDENTIFICATION OF MEDICINAL PRODUCTS - DATA ELEMENTS AND STRUCTURES FOR THE UNIQUE IDENTIFICATION AND EXCHANGE OF REGULATED INFORMATION ON SUBSTANCES (ISO 11238:2012)
Hardcopy , PDF
07-23-2013
English
01-01-2012
For Harmonized Standards, check the EU site to confirm that the Standard is cited in the Official Journal.
Only cited Standards give presumption of conformance to New Approach Directives/Regulations.
Foreword
Introduction
1 Scope
2 Terms, definitions, symbols and abbreviated terms
3 Requirements
Annex A (informative) - Existing identifiers and
molecular structure representations
Bibliography
Gives an information model to define and identify substances within medicinal products or substances used for medicinal purposes, including dietary supplements, foods and cosmetics.
DocumentType |
Standard
|
Pages |
55
|
PublisherName |
National Standards Authority of Ireland
|
Status |
Superseded
|
SupersededBy |
Standards | Relationship |
EN ISO 11238:2012 | Identical |
ISO 11238:2012 | Identical |
ISO 1087-1:2000 | Terminology work Vocabulary Part 1: Theory and application |
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/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 11240:2012 | Health informatics Identification of medicinal products Data elements and structures for the unique identification and exchange of units of measurement |
ISO 8601:2004 | Data elements and interchange formats Information interchange Representation of dates and times |
ISO 11616:2017 | Health informatics — Identification of medicinal products — Data elements and structures for unique identification and exchange of regulated pharmaceutical product information |
ISO/IEC 2382-4:1999 | Information technology Vocabulary Part 4: Organization of data |
ISO 3166-1:2013 | Codes for the representation of names of countries and their subdivisions Part 1: Country codes |
ISO/IEC 7064:2003 | Information technology Security techniques Check character systems |
ISO/HL7 27953-1:2011 | Health informatics — Individual case safety reports (ICSRs) in pharmacovigilance — Part 1: Framework for adverse event reporting |
ISO 1087-2:2000 | Terminology work Vocabulary Part 2: Computer applications |
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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