DIA Europe 2024

Learn how outsourcing can help you reduce regulatory burden in lifecycle management activities and explore the latest trends in pharmacovigilance. IQVIA’s experts guide you through the challenges and solutions for a successful post-approval regulatory lifecycle management partnership and unravel the intricacies of local QPPV.

This session will explore how these crucial elements impact the pharmaceutical industry, shaping the future of healthcare and medicine in the EMEA region.

• Key Takeaways:

  European Lifecycle Management

  • Understand the nuances of regulatory lifecycle management partnerships, its challenges, and opportunities in the ever-evolving pharmaceutical landscape.
• Learn from real case studies about different type of solutions and find which would be the best approach for your company when outsourcing lifecycle regulatory activities on your marketed products.
• Stay updated with the latest trends and developments in European regulatory legislation and how they influence the overall process of post-approval lifecycle management.

Local QPPV

• Explore the pivotal role of a local QPPV and its significance in ensuring drug safety and efficacy in the European context.
• Understand the interplay between local QPPV and regulatory affairs, and how their collaboration impacts drug safety, compliance, and overall regulatory strategy.
• Gain insights into recent and upcoming regulatory changes in the field, ensuring local qualified individuals are well-informed and compliant with evolving standards.
• Understand the need for global collaboration in pharmacovigilance, encouraging local experts to engage with international networks for knowledge sharing and best practices.