On-Demand:
Navigating Global Expansion:
Optimizing Local QPPVs And Regulatory Lifecycle Management For Mid-Size Pharma
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Strategic Pharmacovigilance: Enhancing Global Expansion in Mid-Size Pharma.
Join IQVIA's safety and regulatory experts for an insightful webinar that delves into the interplay between local qualified persons responsible for Pharmacovigilance (QPPVs) and regulatory lifecycle management (LCM) when navigating global expansion. This session will guide you through the challenges and solutions for successful post-approval regulatory LCM and provide best practices for how to navigate the intricacies of local pharmacovigilance.
- Explore the pivotal role and impact of local QPPV and regulatory affairs, and understand how their
collaboration impacts drug safety, compliance, risk management and overall expansion
strategy.
- Learn how to stay ahead of the latest global trends in regulatory legislation.
- Understand the need for global collaboration in pharmacovigilance.
- Examine how mid-size pharma
companies can boost operational efficiency by leveraging advanced safety and
regulatory technologies.
- Analyze real-world examples to identify optimal approaches
for outsourcing lifecycle regulatory and safety activities.
Don’t miss this opportunity to gain valuable insights and strategies for navigating global expansion in the pharmaceutical industry.
Register now →Meet the Speakers
Vera Dinis
Director, Regulatory Affairs and Drug Development Solutions at IQVIA
Ana Pedro
Associate Director, Marketed Production Safety Data Sciences, Safety and Medical at IQVIA
Inspire. Connect. Innovate.
