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An EU-wide approach to HTA: an irrelevant development or an opportunity not to be missed?

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JournalEuropean Journal of Health Economics
DateAccepted/In press - 19 Feb 2019
DateE-pub ahead of print (current) - 14 Mar 2019
Issue number3
Volume20
Number of pages4
Pages (from-to)329-332
Early online date14/03/19
Original languageEnglish

Abstract

An EU-wide cooperation on HTA has been proposed recently by the European Commission, focusing on relative effectiveness assessment (REA) for pharmaceuticals and medical devices. While a good step in the right direction, this collaborative HTA framework needs to be more explicit and pragmatic about clinical value definition, what constitutes quality of evidence, how is real world evidence handled, whether the same assessment requirements will apply for medical devices as they do for pharmaceuticals, and how to safeguard consistency in REA interpretation. If demand- rather than supply-driven, this initiative can deliver wider benefits: Europe can improve its power in global drug design and development, while Member States will have at their disposal more resources to assess performance of interventions in their healthcare systems.

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© The Author(s) 2019

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