Regulatory Affairs & Life Science

EMA PMS Update: Navigating the New Era of Product Data


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New podcast episode out now! Let’s dive into the latest updates from the European Medicines Agency (EMA) on the Product Management Service (PMS) database — key changes on the XEVMPD migration, deadlines, ISO-IDMP requirements, and their impact on MAHs.

A must-listen for professionals in regulatory affairs across pharma. Don’t miss it!

#regulatoryaffairs #PMS #EMA #pharma #regulatoryconsulting
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Regulatory Affairs & Life ScienceBy Di Renzo Regulatrory Affairs