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This PrimeVigilance webinar explores the key elements of building and maintaining a robust pharmacovigilance system in line with Good Pharmacovigilance Practices (GVP). The session covers the regulatory framework for pharmacovigilance, quality objectives, compliance management, performance monitoring, and the role of the EU QPPV in supporting an effective and compliant PV system. It also provides practical guidance for marketing authorization holders looking to strengthen their pharmacovigilance activities and align with global regulatory expectations. Designed for professionals involved in pharmacovigilance and compliance, this webinar offers valuable insight into developing a resilient, high-quality PV system that supports patient safety and regulatory readiness.

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From ISO 9001:2015 to DIS ISO 9001:2025 – The Main Differences [live webinar]

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