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
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
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.
Module 3: Deep Dive into PMS, eAF, and ESMP
by Dr. Anna Thaidigsmann, Principal Business Consultant, EXTEDO
- PMS
New Timeline and the Challenges for MAHs
Data Quality in xEVMPD and PMS
Enrichment in the PMS PUI or PMS API
- eAF
“Strongly Recommended Use” Phase for All Variations (CAPs & NAPs) – Challenges
Data Quality with Regard to the eAF
- ESMP
Union List of Critical Medicines and the Timelines in the ESMP
How to Enter Product Data on Marketing Status, Pack Size, Manufacturers, and Supply
MSSG-Led Preparedness and Crisis Events
This event is part of a five-day course. For more information on the course and booking, please visit: Aufbauwissen für Regulatory Affairs Manager*innen