As a regulatory professional, staying informed about the upcoming events at the European Medicines Agency (EMA) is vital for your work and the advancement of healthcare. With a range of important meetings and industry updates on the horizon, it is essential to plan. In this guide, we have compiled a choice of upcoming events at the EMA that you won’t want to miss. Let’s explore what’s coming up and ensure you’re well-prepared to engage with the critical discussions shaping the industry!
Of course, this list does not cover all the events offered by the EMA. If you're interested in other topics or miss a particular event, you can find the complete list of upcoming events on the EMA website.
We also invite you to meet the EXTEDO team at several events – online or in-person – where we explore the latest developments in regulatory information management and more, learn about new regulatory requirements and standards, and discuss how to approach topics such as eCTD v4 or IDMP. See where you can find us next - we are looking forward to seeing you soon!
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EMA Information Day on submission predictability of initial marketing authorisation, December 2025 |
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eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) training course – 3-day training Wednesday, 17 September 2025, 14:00 - 18:30 (CEST) |
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PMS PUI Training: Product data submission & bulk edit made easy |
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Public webinar on shortages: putting patients first |
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Q&A Clinics for extended EudraVigilance Medicinal Product Dictionary (XEVMPD) service |
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Q&A Clinics for Substance, Organisation, Referentials Management Services (SOR) |
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Questions and answers clinic on Product Management Service (PMS), Product User Interface (PUI), and Application Programming Interface (API) |
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SPOR and XEVMPD status update webinar |