| Greetings!
We are hosting a half-day workshop for professionals working in or alongside the drug submission process. If gaps in your regulatory knowledge are slowing you down, this session is worth your time.
The workshop covers the full New Drug Submission process - from drug development and notice types, through to submission formatting, priority review policy, and the Common Technical Document (CTD). A focused portion addresses eCTD submissions specifically, including where and why applications get screened out before they ever reach review.
It is particularly relevant for regulatory affairs specialists, drug development professionals, quality assurance personnel, and anyone involved in the preparation or filing of new drug submissions.
By the end of the session, you will have a clear, working understanding of what a compliant submission looks like, how the approval process is structured, and where most applicants go wrong. | 
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