| Greetings!
The regulatory submission process for new drugs is a critical step in bringing innovative treatments to market. To help industry professionals, students, and those new to Regulatory Affairs understand the fundamentals of this process, AAPS Pharma is offering a free online workshop on the New Drug Submission (NDS) process.
This session provides an overview of Health Canada’s regulatory expectations, covering the Common Technical Document (CTD) structure, eCTD format, key documentation requirements, and the importance of pre-submission meetings. Participants will gain insights into the general steps of preparing and submitting an NDS and how regulatory submissions impact the pharmaceutical landscape.
Designed for individuals entering the field of Regulatory Affairs or those seeking to understand the basics of drug submissions, this workshop is particularly beneficial for professionals working in pharmaceuticals, healthcare, quality assurance, and drug development. Whether you are looking to advance your career or simply expand your knowledge, this session will equip you with the foundational skills needed to navigate the regulatory submission process.
Registration is open, and all participants will receive a certificate of attendance upon completion. Spaces are limited, so secure your spot today! | 
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