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Duplicated extension content project

Status: Complete

In the second quarter of 2025, concepts from the substance hierarchy that were used to model clinical drugs were collected from nine National Release Centers. These concepts and their terms were compared amongst each other and the international release.   Of the 80 concepts that were found in multiple submissions, 30 were duplicate to current international concepts; almost 50 duplicates were found amongst two or more countries. However, four of these duplicates were rejected as organisms.  Countries that had concepts with the earliest effective times were notified of the selection of their respective concept IDs.  These concepts were promoted and were released into the international edition starting in the 1 August release and finishing in the 1 October 2025 release.  

 

Single promotions project

Status: In progress

Substance concepts used to model clinical drugs and published only within a single extension were collected from nine NRCs for a total of 880 concepts. These were compared to the international release to check for duplication.  Then, SNOMED International staff performed a high-level overview of immediately recognizable issues that could prevent concepts from being internationally applicable.  NRCs were asked to further narrow down the list to only those applicable to the international edition of SNOMED CT.  This process is currently underway.  Promotion of approved concepts is currently in progress.


Extensions identified with substances:

Extension Point(s) of Contact
Argentina
Austria


Australia
Canada Julie Boutin 
India
Norway Hanne Johansen 
Spain
UK
Uruguay
US

Supporting Documents:

Document Link & Details
Combined Substances Worksheet

Combined List June 10th (requires access request) Updated to include more countries June 10th

Tabs:

  • Single Count Substances: List of substances that currently exist in one extension. 
    • Action
      • Each country representative has been sent a link to a spreadsheet with the list of substances within their extension which have been used to model medicinal products.  Please review the substances for relevance in the international edition.  Column B has been provided for comments.  
  • Coincidences pending resolution: Substances in multiple countries where promotion will be required
    • Action:
      • SNOMED International is progressing (CRS for Managed Service or RF2 import for non-Managed Service)
  • Coincidences already resolved: Substances in extensions where there is an International concept
    • Action: Individual extensions to review and inactivate extension concept as there is an International concept. 
Review of Worksheet and Guidance for Extensions


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2 Comments

  1. Dear members of the DEUSG, 

    I sent a message using the SHARE function hereon but just to make sure you are in the know, I will repeat the message here.

    In order to streamline the process: Please do not submit any CRS requests for substance content at this time whether for net new, or content for promotion, or change requests. 

    We have all the content from extensions and are continuing our review. Please complete review of any content you own. Following review, we will promote these concepts via the INFRA ticket system directly into the Authoring Platform. We track progress and will provide feedback in the google sheet and at the next meeting. -


    Thanks for your co-operation and understanding. 

    Monica

  2. Dear Monica,

    We fully understand the importance of streamlining the process and avoiding duplication. However, the Spanish NRC submits monthly CRS requests specifically for new active substances needed to model newly created MP containing concepts representing medicines recently authorized at the EU level and commercialized in Spain. If we are unable to submit these requests, we are forced to create these concepts in our national extension and this approach increases the risk of duplication across extensions, exacerbating the problem we are trying to resolve.

    Therefore, we kindly ask you to reconsider accepting CRS submissions for new active substances, provided we verify that these concepts are present neither in the International Edition nor in other national extensions. Each request is accompanied by the EMA Summary of Product Characteristics as supporting documentation.

    Thank you for your understanding and consideration.

    Marta Pavón Garrido

    Head of Service

    Spanish SNOMED CT National Release Center