Whether you’re a regulatory affairs professional, quality assurance specialist, or someone involved in drug submissions, this Level 2 workshop offers invaluable tools to elevate your career. It’s also a great fit for professionals who have completed the Level 1 session or possess foundational knowledge of CTD and eCTD formats.
Participants will gain hands-on knowledge of advanced regulatory requirements and practical skills to manage pre-submission meetings, respond to Health Canada inquiries, and ensure compliance. By the end of the session, you’ll be equipped with actionable strategies to excel in your field. |
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