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SRPS EN ISO 11616:2014

Health informatics - Identification of medicinal products - Data elements and structures for the unique identification and exchange of regulated pharmaceutical product information (ISO 11616:2012)

Oct 31, 2014
95.99   Withdrawal of Standard   Jun 28, 2018

General information

95.99     Jun 28, 2018

ISS

I215

European Norm

35.240.80  

English  

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Scope

ISO 11616:2012 is intended to provide specific levels of information relevant to the identification of a medicinal product or group of medicinal products. It defines the data elements, structures and relationships between data elements that are required for the exchange of regulated information, in order to uniquely identify pharmaceutical products. This identification is to be applied throughout the product lifecycle to support pharmacovigilance, regulatory and other activities worldwide. In addition, ISO 11616:2012 is essential to ensuring that pharmaceutical product information is assembled in a structured format with transmission between a diverse set of stakeholders. This ensures interoperability and compatibility for both the sender and the recipient.

Life cycle

NOW

WITHDRAWN
SRPS EN ISO 11616:2014
95.99 Withdrawal of Standard
Jun 28, 2018

REVISED BY

PUBLISHED
SRPS EN ISO 11616:2018

Related project

Adopted from EN ISO 11616:2012

Adopted from ISO 11616:2012 IDENTICAL