ISO 11615:2017

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

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

Digital Document2017 edition2017Purchase Options

Referenced standards

ISO 1087-1:2000ISO 11238:2012ISO 11239:2012ISO 11240:2012ISO 11616:2012ISO 21090:2011ISO 3166-1:2013ISO 639-1:2002ISO 8601:2004ISO/HL7 27953-1:2011ISO/HL7 27953-2:2011ISO/IEC 11404:2007ISO/IEC 15415:2011ISO/IEC 15416:2016ISO/IEC 5218:2004ISO/IEC TR 24720:2008ISO/IEC TR 29158:2011ISO/TS 16791:2014ISO/TS 19844:2016ISO/TS 20440:2016ISO/TS 20443:2017ISO/TS 20451:2017
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ISO 11615:2017

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

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

ISO 11615:2017 establishes definitions and concepts and describes data elements and their structural relationships, which are required for the unique identification and the detailed description of Medicinal Products.

Taken together, the standards listed in the Introduction define, characterise and uniquely identify regulated Medicinal Products for human use during their entire life cycle, i.e. from development to authorisation, post-marketing and renewal or withdrawal from the market, where applicable.

Furthermore, to support successful information exchange in relation to the unique identification and characterisation of Medicinal Products, the use of other normative IDMP messaging standards is included, which are to be applied in the context of ISO 11615:2017.

Edition2017
Published Date2017
Published ByInternational Standardization Organisation
Page Count79