Unlocking Continued Revenue And Growth From Established Products

Tap into deep expertise on optimizing post-approval regulatory maintenance for your mature biopharma assets. Join Chris Englerth, Director of Global Consulting Services, as he moderates a discussion with regulatory affairs specialist Paula King. Paula shares invaluable perspectives drawn from extensive experience, focusing on strategies that drive efficiency and market success.

This session dissects real-world scenarios, including a global pharmaceutical leader's journey to achieving 20% cost reduction and a specialty developer's effective use of outsourcing to boost market presence. Understand the critical challenges and discover practical best practices you can implement immediately. Watch the on-demand webinar now to learn more.