Tunisian eCTD Regulations: PLG Webinar Overview

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!

Register now to secure your place and get practical guidance for your upcoming eCTD submissions

Register here