For decades, costly regulatory issues bore witness to pharma’s reactive approach to quality. Billion-dollar consent decrees, caused by fundamental quality failures, drove some manufacturers out of business, while regulators continued to find fault with practices ranging from inadequate CAPA and root-cause analysis to insufficient contract partner oversight.

Learn how Veeva can help CDMOs and Generics manufacturers.

R&D and Quality Summit Europe - Powerful Community, Fresh Ideas

Madrid | 4–5 June, 2025

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