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Overcoming The Manufacturing and Regulatory Challenges for Gene Therapies: From Bench to Patients

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Download key takeaways from this illuminating event, in your free event summary from Pharma Ignite, presented in partnership with Thermo Fisher Scientific.


Capture critical insights into:


  • The most significant factors to consider when developing CGTs for rare diseases
  • Regulatory requirements for the FDA and the EMA and how they differ
  • What to focus on to attain success with FDA and EMA
  • The key for streamlining development and minimizing costs for future cell and gene therapy development


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