CONFERENCE OBJECTIVES
- Understand GCC and UAE eSubmission Roadmap and mandatory switch to eCTD
- Learn how to compile, hyperlink, publish and validate your regulatory submissions
- Gain practical eCTD Submissions knowledge during the interactive hands-on sessions and workshop.
TARGET AUDIENCE
- Regulatory Affairs
- Dossier Management
- e-Submission
- Pharmacovigilance
- Data & Document Management
