In this comprehensive training course learn contemporary principles, regulatory expectations, and practical approaches to drug safety and pharmacovigilance in key regulatory jurisdictions, with a focus on the US and EU. The course curriculum is designed for the basic to intermediate level professional, and the topics will span the lifecycle of traditional innovative medicinal products, from first-in-human through the post-marketing phase. This blended learning course employs a mixture of pre-course online learning, informative instructional sessions, real-world case studies, and hands-on interactive exercises where learners can apply what they learn.
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