{"id":17151,"date":"2025-08-25T15:41:35","date_gmt":"2025-08-25T13:41:35","guid":{"rendered":"https:\/\/www.pharmaeducationcenter.it\/?post_type=product&#038;p=17151"},"modified":"2026-06-11T10:59:31","modified_gmt":"2026-06-11T08:59:31","slug":"eu-regulatory-affairs-basic-training","status":"publish","type":"product","link":"https:\/\/www.pharmaeducationcenter.it\/en\/trainings\/regulatory-affairs\/eu-regulatory-affairs-basic-training\/","title":{"rendered":"EU Regulatory Affairs &#8211; basic training"},"content":{"rendered":"<p>The \u201cBasic Training in European Regulatory Affairs\u201d course will help you gain an understanding of the regulatory requirements for obtaining marketing approval for healthcare products, the fundamentals of drug development, EU law and guidelines, and key regulatory interactions.<\/p>\n<p>You will learn about various modules of the dossier, common technical document, eCTD and online platforms. 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