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Towards Better Pharmaceutical Provision in Europe-Who Decides the Future?

Denis HorganTanja SpanicKathi ApostolidisCurigliano GiuseppeJoanna Chorostowska-WynimkoHans-Peter DaubenJonathan A LalRafal DziadziuszkoChristine Mayer-NicolaiMarta KozaricBengt JönssonIñaki Gutierrez-IbarluzeaMarie-Helene FandelRuth Lopert
Published in: Healthcare (Basel, Switzerland) (2022)
Significant progress has been achieved in human health in the European Union in recent years. New medicines, vaccines, and treatments have been developed to tackle some of the leading causes of disease and life-threatening illnesses. It is clear that investment in research and development (R&D) for innovative medicines and treatments is essential for making progress in preventing and treating diseases. Ahead of the legislative process, which should begin by the end of 2022, discussions focus on how Europe can best promote the huge potential benefits of new science and technology within the regulatory framework. The challenges in European healthcare were spelled out by the panellists at the roundtable organised by European Alliance for Personalised Medicine (EAPM). Outcomes from panellists' discussions have been summarized and re-arranged in this paper under five headings: innovation, unmet medical need, access, security of supply, adapting to progress, and efficiency. Some of the conclusions that emerged from the panel are a call for a better overall holistic vision of the future of pharmaceuticals and health in Europe and a collaborative effort among all stakeholders, seeing the delivery of medicines as part of a broader picture of healthcare.
Keyphrases
  • healthcare
  • human health
  • risk assessment
  • public health
  • climate change
  • current status
  • health information
  • palliative care
  • transcription factor
  • advance care planning
  • quality improvement
  • health promotion