Overview
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 life cycle of traditional innovative medicinal products, from first-in-human through the postmarketing phase. This blended learning course employs a mixture of precourse online learning, informative instructional sessions, real-world case studies, and hands-on interactive exercises where learners can apply what they learn.
Join us at the co-located Boston DIA Member Appreciation Reception and Kickoff for DIA 2018 on August 14, 5:30-7:45PM!
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