Implementing ISO IDMP: introduction to SPOR data services

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TitleImplementing ISO IDMP: introduction to SPOR data services
Date04/08/2016 - 04/08/2016
LocationEuropean Medicines Agency, London, UK
SummaryThis webinar will support industry in understanding the substance, product, organisational and referential (SPOR) data services and related impacts. The European Medicines Agency (EMA) is establishing these business services for the central management and supervision of data in each of the four SPOR areas to facilitate the implementation of the ISO standards for the identification of medicinal products (IDMP). Following a phased implementation, pharmaceutical companies will be required to submit data on medicines to EMA in accordance with these formats and terminologies.

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Name Language First published Last updated
Presentation - Introduction to SPOR data services (English only) 2016-08-16  

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Content outline:

  • explanation of ISO IDMP, why the standards are needed, and how they link to SPOR;
  • benefits and high level changes brought about by the SPOR project;
  • timelines;
  • engagement approach and plan;
  • referentials and organisations operating models;
  • supporting material.