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Stay Up to Date with our Upcoming Events!

Webinar: The eCTD v4 Upgrade: End-to-End Publishing, Transition & Conversion Services

Regulatory deadlines are fixed, but eCTD v4 introduces new complexity and workload for submission teams. Join our Publishing Services experts to learn how dedicated eCTD v4 publishing support ensures compliant, on-time eCTD v4 submissions, e.g. to EMA or the US FDA.

Webinar: Japan eCTD v4: Timelines, Specification and Practical Implications for Life Sciences Companies

Discover the key regulatory updates, technical differences, and best practices for implementing eCTD v4 in Japan. From navigating Japan-specific adaptations to mastering efficient submission workflows, this session equips life sciences companies with the insights they need to succeed.

Event: DIA Europe 2026 - Meet the EXTEDO team!

Together, we experience Sustainability, Innovation, and Collaboration - join us in Rotterdam!

Webinar: The EMA eCTD v4 Pilot Explained: Key Concepts, Industry Readiness and Forward Compatibility

EMA's move toward eCTD v4 is shaping the future of agency and industry alike. Learn the core concepts of the eCTD v4 model, explore the EMA’s approach, and gain valuable insights from eCTD v4 pilot projects.

Event: Pharmacovigilance World 2026: Meet the EXTEDO team

Let's meet in London to drive Excellence in Drug Safety & Pharmacovigilance together.