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BSI - BS EN ISO 11616

Health informatics - Identification of medicinal products - Data elements and structures for the unique identification and exchange of regulated pharmaceutical product information

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Organization: BSI
Publication Date: 31 January 2018
Status: active
Page Count: 44
ICS Code (IT applications in health care technology): 35.240.80

Document History

BS EN ISO 11616
January 31, 2018
Health informatics - Identification of medicinal products - Data elements and structures for the unique identification and exchange of regulated pharmaceutical product information
A description is not available for this item.
BS EN ISO 11616
November 30, 2012
Health informatics - Identification of medicinal products - Data elements and structures for the unique identification and exchange of regulated pharmaceutical product information
A description is not available for this item.

References

This document references:
ISO/HL7 27953-1 - Health informatics — Individual case safety reports (ICSRs) in pharmacovigilance — Part 1: Framework for adverse event reporting
Published by ISO on December 1, 2011
A description is not available for this item.
This document references:
ISO TS 19844 - Health informatics - Identification of medicinal products (IDMP) - Implementation guidelines for ISO 11238 for data elements and structures for the unique identification and exchange of regulated information on substances
Published by ISO on July 1, 2018
This document is used in the implementation of ISO 11238. This document defines substances based on their scientific identity (i.e. what they are) rather than on their use or method of production....
This document references:
ISO TS 20440 - Health informatics - Identification of medicinal products - Implementation guide for ISO 11239 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
Published by ISO on June 1, 2016
This Technical Specification describes data elements and structures for the unique identification and exchange of regulated information on pharmaceutical dose forms, units of presentation, routes of...
This document references:
ISO 3166-1 - Codes for the representation of names of countries and their subdivisions - Part 1: Country code
Published by ISO on August 1, 2020
This document specifies basic guidelines for the implementation and maintenance of country codes. This code is intended for use in any application requiring the expression of current country names in...
This document references:
ISO TS 19844 - Health informatics - Identification of medicinal products (IDMP) - Implementation guidelines for ISO 11238 for data elements and structures for the unique identification and exchange of regulated information on substances
Published by ISO on July 1, 2018
This document is used in the implementation of ISO 11238. This document defines substances based on their scientific identity (i.e. what they are) rather than on their use or method of production....
This document references:
ISO TS 20440 - Health informatics - Identification of medicinal products - Implementation guide for ISO 11239 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
Published by ISO on June 1, 2016
This Technical Specification describes data elements and structures for the unique identification and exchange of regulated information on pharmaceutical dose forms, units of presentation, routes of...
This document references:
ISO 3166-1 - Codes for the representation of names of countries and their subdivisions - Part 1: Country code
Published by ISO on August 1, 2020
This document specifies basic guidelines for the implementation and maintenance of country codes. This code is intended for use in any application requiring the expression of current country names in...
This document references:
ISO/HL7 27953-1 - Health informatics — Individual case safety reports (ICSRs) in pharmacovigilance — Part 1: Framework for adverse event reporting
Published by ISO on December 1, 2011
A description is not available for this item.
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