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Effective Strategies for Post-approval Lifecycle Management and Local Pharmacovigilance
Unlock the secrets of Post-Approval LCM and LQPPV with IQVIA's expert white paper
Jul 10, 2024
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Discover IQVIA's insights on Post-Approval Lifecycle Management and Local Pharmacovigilance. This white paper highlights the journey beyond Marketing Authorization Approval, emphasizing the need for expert management of renewals, variations, and regulatory information. It addresses the challenges of global regulatory differences and the EU's pharmaceutical legislation reform. Learn about creating a resilient regulatory strategy with stakeholder input, transparent communication, and defined roles. Explore the advantages of partnering with regulatory services providers for global expansion, market application expansion, and strategic pharmacovigilance management. Gain access to Local Qualified Persons for Pharmacovigilance (LQPPVs) and leverage technology for efficient and compliant post-approval processes. Ensure patient safety and regulatory adherence with IQVIA's comprehensive approach.

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