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. 2019 Jun;19(3):251-261.
doi: 10.1080/14737167.2019.1575730. Epub 2019 Feb 15.

Proposal for a regulation on health technology assessment in Europe - opinions of policy makers, payers and academics from the field of HTA

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Free article

Proposal for a regulation on health technology assessment in Europe - opinions of policy makers, payers and academics from the field of HTA

Patricia Vella Bonanno et al. Expert Rev Pharmacoecon Outcomes Res. 2019 Jun.
Free article

Abstract

In January 2018 the European Commission published a Proposal for a Regulation on Health Technology Assessment (HTA): 'Proposal for a Regulation on health technology assessment and amending Directive 2011/24/EU'. A number of stakeholders, including some Member States, welcomed this initiative as it was considered to improve collaboration, reduce duplication and improve efficiency. There were however a number of concerns including its legal basis, the establishment of a single managing authority, the preservation of national jurisdiction over HTA decision-making and the voluntary/mandatory uptake of joint assessments by Member States. Areas covered: This paper presents the consolidated views and considerations on the original Proposal as set by the European Commission of a number of policy makers, payers, experts from pricing and reimbursement authorities and academics from across Europe. Expert commentary: The Proposal has since been extensively discussed at Council and while good progress has been achieved, there are still divergent positions. The European Parliament gave a number of recommendations for amendments. If the Proposal is approved, it is important that a balanced, improved outcome is achieved for all stakeholders. If not approved, the extensive contribution and progress attained should be sustained and preserved, and the best alternative solutions found.

Keywords: EUnetHTA; European legislation; Member States; cross border agreements; joint collaboration on HTA.

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