On-Demand: Regulatory Operations In 2024: Emerging Trends in Lifecycle Management, Labeling And Publishing 

View IQVIA’s regulatory experts in a panel discussion on growing trends and opportunities in regulatory strategy, lifecycle management, labeling, and publishing. 

Discover the critical regulatory developments on the horizon for biotechs and mid-to-large pharma companies.

You will learn:

• Proactive lifecycle planning strategies to maximize the impact of a product on patients, providers and their own bottom line
• Future practices for optimizing end-to-end labeling and publishing services with a proven delivery model to enable higher efficiency, workforce flexibility, high-quality and timely submissions
• How mid-size pharma can streamline their end-to-end regulatory strategy and global regulatory operations
• Where and when to use artificial intelligence and machine learning to streamline regulatory operations

Don't miss out on this opportunity to gain critical knowledge to prepare for the future of regulatory operations and lifecycle management. 

Expert panelists include:

Marcela Mino

Senior Director, Regulatory Affairs & Drug Development, IQVIA

Rama Mohan Rao Chikkam

Senior Director, Global Regulatory Operations & APAC RA, IQVIA

Keith McDonald

Head of Drug Development Strategy, Regulatory Affairs & Drug Development Solutions, IQVIA

David Cameron

Senior Director, Regulatory Affairs & Drug Development Solutions, IQVIA