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Data Transparency Autumn Event – Call For Speakers

We’re excited to announce that Call for Speakers for the Data Transparency Autumn Event, 15–17 September 2026, is open! Explore the list of topics and consider how your insights can shape the agenda. 

Submit your 150-word abstract by 8 May.

The Data Transparency Working Group invites abstract submissions for its upcoming multi‑day virtual event, taking place 15–17 September 2026 at 10:00–12:30 (EDT) / 15:00–17:30 (BST) / 16:00–18:30 (CEST).

The event will focus on the evolving landscape of clinical data transparency, including approaches to data sharing, anonymisation, governance and enabling responsible access to clinical data.

Focus your submission on these central themes and submit an abstract by 8 May to contribute to the discussion.

Click here for more information.

Info

Submit Abstract Here

Real World Data Autumn Event – Call For Speakers

We’re excited to announce that Call We’re excited to announce Call for Speakers for the the Real World Data Autumn Event, 30 September–1 October 2026, is open! Explore the list of topics and consider how your insights can shape the agenda. 

Submit your 150-word abstract by 8 May

Evidence Working Group’s second multi‑day virtual event is now open! Taking place 30 September – 1 October 2026, from 09:00–11:30 (EDT) / 14:00–16:30 (BST) / 15:00–17:30 (CEST).

Submit your abstract by 8 May for the chance to present.

Focus your submission on these central themes:

  • Optimising the Generation of Real‑World Evidence with NLP & AI

  • Digital Endpoints Generated from Real‑World Data

  • Data Sources, Lineage and Provenance

  • Vendor–Sponsor Governance and Alignment

  • Any Other Theme that Tackles the Challenges in Using Real‑World Data

Click here for more information.

Info

Submit Abstract Here

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Optimizing the Use of Data Standards

The SDTM ADaM Implementation FAQ project within the Optimizing the Use of Data StandardsWorking Group has published a new response to a question regarding SDTM/ADaM IG Nuances. View the team's response to the following question here.  

‘CTCAE Upversioning – When should a sponsor organisation decide to upversion CTCAE, DAIDS, or any other toxicity grading standards? How should sponsors handle pooled analyses with varying grading scales?'

Do you have a (FAQ project based) question? Send your questions to the team by emailing workinggroups@phuse.global. 

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