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.
Speakers
Jay Gandecha, Senior Director, Regulatory Affairs, IQVIA
Jay Gandecha is a recognized authority in global regulatory affairs and post-marketing compliance, currently serving as a Senior Director within IQVIA’s Regulatory Affairs & Drug Development Solutions, where he helps sponsors harmonize lifecycle management and regulatory operations across markets. With 20+ years in life sciences and recognition as a Chartered Scientist, Jay has led cross functional programs that streamline submissions, labeling and maintenance activities while strengthening governance and inspection readiness for complex portfolios. He holds a BSc (Hons) in Pharmaceutical and Chemical Sciences from Liverpool John Moores University.
Message Presenter
Ana Pedro Jesuíno, Director of Marketed Product Safety, IQVIA
Ana Pedro Jesuíno is a seasoned leader in global pharmacovigilance and regulatory compliance, currently Global Head for IQVIA’s Local QPPV Network. With 15+ years’ experience in CRO and the pharmaceutical industry, Ana has overseen safety systems in 50+ markets, driving process harmonization and inspection readiness. She holds a Master’s in Pharmaceutical Sciences and leads cross-functional teams and global training programs.
Who Should Attend?
This webinar will appeal to:
- Regulatory Affairs Leaders and Compliance Officers
- Pharmacovigilance and Drug Safety Professionals, including QPPVs and Local QPPVs
- Labeling and Lifecycle Management Specialists
- Affiliate Managers and Regional Regulatory Leads
- Technology and Innovation Leaders focused on AI and automation in life sciences
What You Will Learn
Attendees will gain insight into:
- How integrating safety and regulatory functions across the enterprise can create unified governance, reduce duplication and enable faster, more consistent decision-making globally
- Approaches to flexible staffing and adaptive resourcing that address workload peaks and local expertise gaps, without requiring permanent in-country teams
- Practical applications of AI and automation in cross-functional post-marketing workflows such as pharmacovigilance, labeling updates and regulatory submissions, using a technology-agnostic approach
- Engagement models that allow organizations to tailor solutions to their current needs, whether focusing on LQPPV, LCM or a combined strategy
Xtalks Partner
IQVIA
IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. IQVIA creates intelligent connections to deliver powerful insights with speed and agility — enabling customers to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. With approximately 82,000 employees, IQVIA conducts operations in more than 100 countries. Learn more at www.iqvia.com.
You Must Login To Register for this Free Webinar
Already have an account? LOGIN HERE. If you don’t have an account you need to create a free account.
Create Account