Topics
- Understand eCTD concept and structure
- Review the process that led to the development of the CTD
- Understand how the eCTD organizes study files
- Become familiar with the underlying technology used in the eCTD
- Get a glimpse into the challenges and logistics of submission management
- Learn about lifecycle management advantages of the eCTD
The Introduction to the Electronic Common Technical Document 2012 brings together attendees from Pharma, Biotech and Medical Device companies including Regulatory Affairs, Medical Writing, IT Management, Document Management, Submission Management, Compliance and Professionals who are new to eCTD.
