The FDA is looking to mandate electronic submissions in the next few years. At the same time, they and other regulators are looking to upgrade the eCTD standard. Why would the FDA mandate electronic submissions and change the standard at the same time?
Jason Rock, Chief Technical Officer at GlobalSubmit, will provide greater insight into this topic during a free educational webinar jointly hosted by Cato Research and GlobalSubmit, “Background and Drivers to the eCTD Next Major Version / Regulated Product Submission”, on Thursday, October 4th at 1:00 p.m. EDT.
During this discussion, Jason will provide detailed reasons why a new standard was created, the timelines when the standard will be complete, what each of the agencies’ plans are, and the major differences between eCTD version 3 and 4.
Top 3 Learning Objectives:
- Why eCTD v4 was developed
- What the agency’s plan is for eCTD v4
- What’s the difference between eCTD v4 and eCTD v3
Register now for this free webinar!
UPDATE: The webinar slides are available for download here.