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The Legal Framework for Public-Private Partnerships in Drug R&D.

Thomas Hirse
Published in: Handbook of experimental pharmacology (2024)
Public-private partnerships in drug R&D have great potential for driving innovation. They can bridge between excellent fundamental research and development and commercialization of innovative medicines to address unmet needs for the therapy of severe diseases in the interest of public health and human welfare. Therefore, public-private partnerships in drug R&D are promoted and publicly funded by governments and the European Commission. Nonetheless, they need to comply with legal requirements, particularly stemming from State aid law and competition law. Those requirements do not only protect a fair competition, but rather also further open information exchange as well as fair sharing of risks and fair participation in gains and results with the goal of having a successful collaboration and increasing the chance of successful commercialization of pharmaceutical innovations.
Keyphrases
  • healthcare
  • public health
  • health insurance
  • adverse drug
  • global health
  • mental health
  • endothelial cells
  • health information
  • drug induced
  • minimally invasive
  • induced pluripotent stem cells