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Panel: Engaging regulators early – The key to accelerating ATMP development

04 Sep 2025
Theatre 1
R&D, clinical innovation & translation
  • Best practices for early interactions with EMA, FDA, MHRA etc. 

  • How proactive regulatory engagement reduces delays and de-risk trials 

  • Lessons learned from companies that successfully navigated approval 

 

Chairperson
Anna Koptina, Head of Regulatory Affairs - Elicera Therapeutics
Speakers
Benjamin Dewees, Senior Vice President of Regulatory Affairs - Artiva Biotherapeutics
Magda Papadaki, Executive Director - MSD
Aneta Tyszkiewicz, Director Digital and Data - European Federation of Pharmaceutical Industries and Associations