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Cell and Gene Therapy 2025

Cell and Gene Therapy 2025


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This event will focus on the latest progress in precision genome editing, novel delivery vectors, allogeneic cell therapies and the journey from laboratory research to clinical application, offering insights into the future of personalized medicine.


Key Learning Objectives:
  • Gain insights into the latest breakthroughs in precision genome editing technologies and their implications for therapeutic development.
  • Learn about the latest vector delivery systems for gene therapies and their role in enhancing efficacy and safety.
  • Understand the critical steps involved in translating laboratory research into clinical-grade cell and gene therapies.
  • Explore how innovations in cell and gene therapy are paving the way for more precise, individualized treatment options.


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Who Should Attend:
  • Biotechnology and biopharmaceutical experts looking to stay ahead in this rapidly evolving field. 
  • R&D scientists focused on genome editing, cell therapy and translational medicine.
  • Aspiring graduates looking to further their expertise. 


What Past Attendees are Saying:
  • "Very well organized. It was a right mix of expertise around the central topics Covered all key aspects expected." Staff Scientist
  • "It was truly one of the best events I have ever attended. From the speakers to the topics to the content, everything was simply mind-blowing. I must commend the organizers for curating such an enriching experience." - Student

Speakers to be Announced Soon!

Panel Speakers
A picture of Mike Ward
Mike Ward
Head of Thought Leadership, Life Sciences & Healthcare
Clarivate
A picture of Matthew Arnold
Matthew Arnold
Principal Analyst
Clarivate
Speakers
A picture of Matthew Porteus, MD
Matthew Porteus, MD
Professor of Definitive and Curative Medicine and of Pediatrics
Stanford University
A picture of Justin Eyquem, PhD
Justin Eyquem, PhD
Assistant Professor of Medicine
University of California San Francisco
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