Abstract
After 3 years of co-design with stakeholders and EU regulatory partners, the European Medicines Agency's Regulatory Science to 2025 strategy has been finalized. Here, we highlight the core recommendations that stakeholders deem most significant to advance evidence generation.
Original language | English |
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Pages (from-to) | 293-294 |
Number of pages | 2 |
Journal | Nature Reviews Drug Discovery |
Volume | 19 |
Issue number | 5 |
DOIs | |
Publication status | Published - 1 May 2020 |
JEL classifications
- i18 - "Health: Government Policy; Regulation; Public Health"
- o30 - "Technological Change; Research and Development; Intellectual Property Rights: General"
Keywords
- Regulation
- Medicines
- Intellectual Property
- Science
- R&D
- European Union