Regulatory Submissions in eCTD - The Case of New Regulations in Tunisia

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.

• 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

🗓️ 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!