| Greetings!
Advance your regulatory affairs expertise with AAPS Pharma’s upcoming Level 2 workshop on Drug Product Submission (NDS) in CTD and eCTD format. Tailored for professionals who have a foundational understanding of regulatory submissions, this training builds directly upon the concepts introduced in Level I, diving deeper into the technical and strategic elements of advanced Health Canada submissions.
Through real-world case studies and in-depth guidance, participants will gain practical insight into Modules 3, 4, and 5, learning how to effectively handle quality documentation, nonclinical study reports, and clinical data. The workshop also focuses on how to manage the entire submission lifecycle—from conducting successful pre-submission meetings to addressing regulatory queries and navigating Health Canada’s expectations.
Whether you’re working in regulatory affairs, clinical research, or quality assurance, this session will equip you with advanced tools and strategies to streamline your submission process. You’ll explore how to format documents for the eCTD platform, maintain compliance throughout the lifecycle, and leverage electronic submissions for efficiency and clarity.
All attendees will receive a certificate of participation upon completion. Spaces are limited and registration will close one week prior to the event. We invite you to take the next step in your professional development and join a community of experts advancing pharmaceutical regulatory excellence.
Ready to elevate your regulatory skillset? | 
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