Explore the evolving regulatory landscape for protein-based therapeutics in this on-demand webinar. Gain strategic insights into Chemistry, Manufacturing, and Controls (CMC) requirements across the product lifecycle—from preclinical development to market approval and beyond.

Through case studies and practical examples involving complex products like ADCs, learn how Lonza supports clients with integrated regulatory services and strategic guidance. The webinar emphasizes the importance of regulatory expertise, cross-functional collaboration, and adaptability in today’s complex global environment.

Learning Objectives

  • Understand the value of strategic regulatory planning across all development stages
  • Apply evolving regulatory pathways and tailor submissions to agency expectations
  • Recognize how partnering with experienced CDMOs like Lonza enhances regulatory readiness and lifecycle management
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