DIA
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Pragmatic Approaches to Drug Safety Across the Premarketing and Postmarketing Continuum

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Overview 

This basic to intermediate-level course focuses on pharmacovigilance of traditional medicinal products intended for human use. Topics will span investigational and marketed products in clinical trials, post-marketing studies, and under conditions of actual use in real-world health care settings.  Late breaking regulatory changes, pertaining to the EU will be presented.  Attendees will gain a detailed understanding of safety and pharmacovigilance obligations and best practices.

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