With the next version of eCTD (Electronic Common Technical Document) now accepted or soon to be accepted by major health authorities for regulatory submissions, organizations must adapt their submission planning, processes, and documentation to be cohesive with this format. A key part of this will be understanding the differences between the new eCTD format (v4.0) and the eCTD version that has been widely used for many years (v3.2.2).

This on-demand webinar offers an in-depth comparison of the eCTD 3.2.2 and eCTD 4.0 submission structure. Our experts discuss the most significant changes and the distinctions that most directly impact submission preparation. Plus, they’ll provide practical guidance on navigating related challenges.

Whether you’re already planning submissions in eCTD 4.0 or getting ready for future possibilities, this webinar will provide the insights you need to stay on the forefront of regulatory submissions.

Key Learning Objectives:

• Identify key structural differences between eCTD 3.2.2 and eCTD 4.0
• Examine the changes that will most directly impact submission preparation
• How to successfully navigate the challenges posed by these changes

eCTD 4.0 marks a significant shift in regulatory submissions. Stay prepared and informed. Sign-up to gain valuable insights and ensure your team is ready for the transition.