EMA Regulatory Science to 2025 - Five goals

On 14 November 2019 the EMA updated its five goals for human medicine regulation

The European Medicines Agency updated the below five goals through to 2025:

  • Catalysing the integration of science and technology in medicines development
  • Driving collaborative evidence generation and improving the scientific quality of evaluations
  • Advancing patient-centred access to medicines in partnership with healthcare systems
  • Addressing emerging health threats and availability/ therapeutic challenges
  • Enabling and leveraging research and innovation in regulatory science
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