Pav is a dynamic and visionary healthcare leader, with 25 years of extensive experience across various safety (and PV) functions, which include senior management and leadership roles within the (PV) discipline. He is recognised as a credible and respected global figure in the industry and remains at the forefront of global PV efforts. He currently holds the position of Director of Pharmacovigilance & UK QPPV at Ipsen Biopharma and serves as the chair of the UK The Association of the British Pharmaceutical Industry (ABPI) Pharmacovigilance Expert Network (PEN) for over seven years, demonstrating his commitment to advancing innovative strategies for patient safety with purpose. Pav is a global advocate of purposeful leadership – he empowers stakeholders through his unique articulation and deliveries enabling positive outcomes. He continues to influence the global landscape through key platforms and expert forums bringing the industry voice to the table enabling many national guidelines and legislation.
Attendees will gain insights into evolving global pharmacovigilance regulations, harmonization efforts, and compliance strategies across diverse markets. Through expert perspectives and case studies, they will explore how to navigate complex regulatory frameworks, align with international guidance, and implement best practices to ensure safety and compliance on a global scale.
As pharmacovigilance becomes more global, data-rich, and digitally enabled, sponsors are rethinking what they need from their vendors—and what true partnership really means. In this forward-looking panel, we’ll explore how sponsors and service providers can move beyond transactional models toward trusted, strategic collaborations built for innovation, resilience, and shared accountability.
Topics will include:
Sponsored by Med Communications, Inc.
Attendees will gain insights into evolving global pharmacovigilance regulations, harmonization efforts, and compliance strategies across diverse markets. Through expert perspectives and case studies, they will explore how to navigate complex regulatory frameworks, align with international guidance, and implement best practices to ensure safety and compliance on a global scale.
Attendees will gain a deep understanding of how AI, machine learning, and automation are revolutionizing pharmacovigilance by streamlining case processing, enhancing signal detection, and driving operational efficiency. They will explore real-world applications, innovative tools, and forward-looking strategies to build trust in AI and future-proof safety operations across the drug development lifecycle.
This fireside chat will deliver a compelling narrative around the potential of AI based tools, focusing on the real (human) foundations of deployment like cultural change and building trust.
Attendees will gain a deep understanding of how AI, machine learning, and automation are revolutionizing pharmacovigilance by streamlining case processing, enhancing signal detection, and driving operational efficiency. They will explore real-world applications, innovative tools, and forward-looking strategies to build trust in AI and future-proof safety operations across the drug development lifecycle.