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New EU Clinical Trial Regulations

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Explore the challenges and benefits for biotechs conducting trials in the EU, and why partnerships are crucial to support the trial journey, as they discuss:

  • EU’s complex transition to CTIS
  • Regulatory and cost differences across EU countries
  • Patient diversity and recruitment
  • Ensuring regulatory compliance
  • Impact of CTR on streamlining processes
  • EMA vs FDA
  • Importance of CRO partnerships with local expertise

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