The Tunisian Drug Master File (DMP) now requires that Marketing Authorization (MA) applications be submitted in eCTD format. To guide companies through this major regulatory shift, Product Life Africa - a member of the ProductLife Group - is hosting a dedicated webinar on eCTD & ePublishing.
With extensive experience supporting global regulatory submissions, PLG is uniquely positioned to help organisations navigate the transition to eCTD with confidence and efficiency.
This online session is crafted for life-sciences professionals seeking to deepen their understanding and gain practical insights they can apply immediately to their submission processes.
What You Will Learn
- Key requirements of the new Tunisian eCTD regulation
- The eCTD publishing process and real-world feedback from experience
- Best practices for compiling and validating an eCTD dossier
- How ProductLife Group can help you become efficient with the eCTD format
When & How
16 December 2025 | 14:00 - 15:30 CET
Format: Free online webinar - in French
Speakers: Fadime Kale, Mariem Kebaier | Moderator: Sarra Blel
Don't miss this opportunity to turn regulatory complexity into opportunity!