EMA (EU)
EVENT
HMA / EMA multistakeholder AI and Data forum: Build trustworthy AI on strong data foundations
Published: 11/12/2026Detected: 11/6/2026
Summary preview
Advances the EU medicines regulatory network’s data and AI agenda by convening regulators and stakeholders to share progress and influence future policy direction across the human and veterinary lifecycle.
Get the full analysis, free
Create a free account to see the complete summary, key takeaways, and why this matters for your products, and to get alerts like this by email.
Create free accountmanufacturing
quality
clinical
safety
labeling
#AI
#data governance
#data quality
#interoperability
#European Medicines Regulatory Network
Official Source Document Source Verified
Access the original document directly from EMA.
More from EMA (EU)
- PMS Q&A Clinic on Product User Interface (PUI) and Application Programming Interface (API) – November 202611/12/2026
- Stakeholder Meeting on the transferable data exclusivity voucher (TDEV) for priority antimicrobials11/12/2026
- Q&A clinic on eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) service - November 202611/12/2026
- Q&A clinic on Substance, Organisation, Referentials Management Services - November 202611/11/2026
- Meeting of the Medicine Shortages Single Point of Contact (SPOC) Working Party11/10/2026