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Is there a need for a centralised, European HTA agency and predictable, transparent European standards?

Related topics: Pharmaceutical/Biotech, Europe, Market Access & HEOR

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Overview
  • How similar are HTA agencies in methods and procedures?
  • Is there a development towards shared standards?
  • What are stakeholders doing to encourage harmonisation/standardisation?
  • Is there a need for a European institution to get the job done?
Speaker

Finn Boerlum Kristensen
Managing Director Science & Policy, Faculty of Health Sciences, University of Southern Denmark
Former EUnetHTA Executive, Committee Chairman and EUnetHTA Secretariat Director

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REMINDER

This is the presenters’ personal opinion and does not necessarily represent true facts, the official views or policy of their organisation, nor the views of Evidence Life Science.