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Location |
TBA
Munich, Germany |
Region | EMEA |
Benefit from in-depth discussions which will allow you to:
• Comprehend how global affairs are transforming the development and commercialization of biologics and biosimilars
• Analyse the global legal and business ramifications of the EMA and FDA biosimilar regulatory pathways
• Understand the significance of regulatory exclusivities in biosimilar development from the perspectives of both originators and biosimilars
• Evaluate the impact of the current SPC landscape and the implementation of the UPC
• Traverse the complexities of U.S. market entry: naming, labeling, and marketing concerns
• Implement winning strategies to prevent compliance breaches of EU competition law
• Learn how AI and data mining accelerate drug discovery and development
2023 Partners
• Dechert
• Patsnap
• Sterne Kessler