| This webinar will delve into the crucial CMC section of a Common Technical Document (CTD), which is essential for regulatory submissions in Canada and the EU. It is tailored for professionals in various industries, including pharmaceuticals, biopharmaceuticals, vitamins, herbals, medical devices, and more.
If you're immersed in the world of regulatory affairs, this training is your golden opportunity. Whether you're a regulatory affairs director, manager, specialist, or working in related roles that are pivotal to ensuring regulatory compliance and product success, this webinar is meticulously crafted to bolster your expertise. Join us to strengthen your regulatory knowledge and gain a competitive edge in the field | 
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