Approved Work Item
ISO/AWI 11615
Health informatics — Identification of medicinal products — Data elements and structures for the unique identification and exchange of regulated medicinal product information
Reference number
ISO/AWI 11615
Edition 3
Approved Work Item
ISO/AWI 11615
88548
A working group has prepared a draft.
Will replace ISO 11615:2017

Abstract

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.

General information

  •  : Under development
    : New project registered in TC/SC work programme [20.00]
  •  : 3
  • ISO/TC 215
  • RSS updates

Sustainable Development Goals

This standard contributes to the following Sustainable Development Goal

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