In this insightful discussion, IQVIA experts will share how organizations can achieve local compliance on a global scale by integrating safety and regulatory functions across the enterprise. Attendees will discover how combining Local Qualified Person for Pharmacovigilance (LQPPV) responsibilities with comprehensive Lifecycle Management (LCM) services creates unified governance, reduces duplication and accelerates decision-making while maintaining flexibility for sponsors who lack dedicated in-country resources.
The featured speakers will also explore how adaptive resourcing models and applied AI can streamline post-marketing activities such as pharmacovigilance workflows, labeling updates and regulatory submissions without locking into proprietary technology. This session will provide practical strategies for balancing compliance obligations with operational efficiency, even in complex multi-country environments.
Register for this webinar to learn how applied AI and adaptive resourcing can support compliant, scalable LQPPV and lifecycle management across global post-marketing operations.
Attendees will learn:
Jay Gandecha, Senior Director, Regulatory Affairs, IQVIA
Ana Pedro Jesuíno, Director of Marketed Product Safety, IQVIA
For more information and to register, click here.
Automate and standardize your regulatory management, from correspondence and commitments to registration and tracking.
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