Join our experts, Maryanne Loscalzo, Associate Director of Reg Ops, and Trevor Standish, Director of Product Management, as they provide an overview of eCTD v4.0.
The world of electronic regulatory submissions is about to change with the introduction of eCTD (Electronic Common Technical Document) v4.0. This latest version of the standard includes updated specifications and guidelines for the preparation and submission of electronic regulatory documents.
During this webinar, we will cover the similarities and differences between the FDA’s eCTD v4.0 and previous versions, as well as the FDA’s current plans for rolling out this new standard. A brief demo of GlobalSubmit Publish will help show exactly how eCTD v4.0 will appear when preparing a submission using this new standard.
Don’t miss this opportunity to learn more about eCTD v4.0 and see the live Q&A session along with polling results. Sign up to watch the webinar today!
