EXTEDO Experts sharing their Expertise - Where to Meet Them
At EXTEDO, we believe that sharing knowledge benefits everyone. That is why we are delighted that our experts are invited to several events to bring their expertise to the audience. We have gathered a few events here where you can meet the EXTEDO experts live or online.
Make sure to mark these dates in your calendar and plan your participation for an extra bit of EXTEDO expertise!
Event Title: "Product Management Service (PMS) information day 2026" Date & Time: , - Organizer: European Medicines Agency (EMA) Location: Online /European Medicines Agency, Amsterdam, the Netherlands/ Live broadcast
Description: The third edition of the Product Management Service (PMS) info day is designed to provide interested stakeholders with a clear understanding of the strategic direction of PMS and how it contributes to the broader Network objectives.
The event starts with a public session from 8:45 to 13:00 (broadcast available from this page and EMA's YouTube channel
After the public session, there will be afternoon discussions exclusively for on-site attendees at the EMA premises.
Event Title: "Enrichment PMS, Multiplikation XEVMPD" within "Regulatory Operations Update - Ihre To-Dos 2026/2027" (in German) Date & Time: Wednesday, 15 July - Thursday, 16 July 2026; 09:00 - 17:00 CEST Organizer: FORUM Institut Location: Online
Description: This seminar provides a comprehensive update on all EMA IT systems relevant to regulatory compliance and their data content. It also offers practical solutions for implementing current and future pharmaceutical data management requirements. Participants may also receive assistance with specific questions.
Event Title: "Modul 3: Deepdive PMS, eAF, ESMP" within "Aufbauwissen für Regulatory Affairs Manager*innen" (Webcast Series, in German) Date & Time: Tuesday, 22 September 2026, 09:00 - 13:00 CEST Organizer: FORUM Institut Location: Online
Description: This modular training program gives you the chance to expand and refresh your knowledge of drug approval. Take advantage of practical webcasts designed specifically for experienced regulatory affairs professionals. All modules are recorded and made available afterward.
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