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Navigating the path towards successful implementation of the EU HTA Regulation: key takeaways from the 2023 Spring Convention of the European Access Academy.
Brinkhuis, Francine; Julian, Elaine; van den Ham, Hendrika; Gianfrate, Fabrizio; Strammiello, Valentina; Berntgen, Michael; Pavlovic, Mira; Mol, Peter; Wasem, Jürgen; Van Dyck, Walter; Cardone, Antonella; Dierks, Christian; Schiel, Anja; Bernardini, Renato; Solà-Morales, Oriol; Ruof, Jörg; Goettsch, Wim.
Afiliação
  • Brinkhuis F; Utrecht WHO Collaborating Centre for Pharmaceutical Policy and Regulation, Division of Pharmacoepidemiology and Clinical Pharmacology, Utrecht University, Utrecht, The Netherlands.
  • Julian E; Secretariat of the European Access Academy (EAA), Hauensteinstr. 132, 4059, Basel, Switzerland. info@euaac.org.
  • van den Ham H; Utrecht WHO Collaborating Centre for Pharmaceutical Policy and Regulation, Division of Pharmacoepidemiology and Clinical Pharmacology, Utrecht University, Utrecht, The Netherlands.
  • Gianfrate F; University of Ferrara, Ferrara, Italy.
  • Strammiello V; European Patients' Forum (EPF), Brussels, Belgium.
  • Berntgen M; European Medicines Agency (EMA), Amsterdam, The Netherlands.
  • Pavlovic M; Medicines Development and Training (MDT) Services, Paris, France.
  • Mol P; Department of Clinical Pharmacy and Pharmacology, University Medical Center Groningen (UMCG), University of Groningen, Groningen, The Netherlands.
  • Wasem J; Institute for Health Care Management and Research, University of Duisburg-Essen, Essen, Germany.
  • Van Dyck W; Healthcare Management Centre, Vlerick Business School, Brussels, Belgium.
  • Cardone A; Cancer Patients Europe' (CPE), Brussels, Belgium.
  • Dierks C; Dierks + Company, Berlin, Germany.
  • Schiel A; Norwegian Medicines Agency (NOMA), Oslo, Norway.
  • Bernardini R; Department of Biomedical and Biotechnological Sciences (BIOMETEC), Section of Pharmacology, University of Catania, Catania, Italy.
  • Solà-Morales O; HiTT Foundation, International University of Catalonia-UIC, Barcelona, Spain.
  • Ruof J; Secretariat of the European Access Academy (EAA), Hauensteinstr. 132, 4059, Basel, Switzerland.
  • Goettsch W; Medical School of Hanover, Hanover, Germany.
Health Res Policy Syst ; 22(1): 74, 2024 Jul 02.
Article em En | MEDLINE | ID: mdl-38956568
ABSTRACT

BACKGROUND:

The European Regulation on Health Technology Assessment (EU HTA R), effective since January 2022, aims to harmonize and improve the efficiency of common HTA across Member States (MS), with a phased implementation from January 2025. At "midterms" of the preparation phase for the implementation of the Regulation our aim was to identify and prioritize tangible action points to move forward.

METHODS:

During the 2023 Spring Convention of the European Access Academy (EAA), participants from different nationalities and stakeholder backgrounds discussed readiness and remaining challenges for the Regulation's implementation and identified and prioritized action points. For this purpose, participants were assigned to four working groups (i) Health Policy Challenges, (ii) Stakeholder Readiness, (iii) Approach to Uncertainty and (iv) Challenges regarding Methodology. Top four action points for each working group were identified and subsequently ranked by all participants during the final plenary session.

RESULTS:

Overall "readiness" for the Regulation was perceived as neutral. Prioritized action points included the following Health Policy, i.e. assess adjustability of MS laws and health policy processes; Stakeholders, i.e. capacity building; Uncertainty, i.e. implement HTA guidelines as living documents; Methodology, i.e. clarify the Population, Intervention, Comparator(s), Outcomes (PICO) identification process.

CONCLUSIONS:

At "midterms" of the preparation phase, the focus for the months to come is on executing the tangible action points identified at EAA's Spring Convention. All action points centre around three overarching themes harmonization and standardization, capacity building and collaboration, uncertainty management and robust data. These themes will ultimately determine the success of the EU HTA R in the long run.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Avaliação da Tecnologia Biomédica / União Europeia / Fortalecimento Institucional / Participação dos Interessados / Política de Saúde Limite: Humans País/Região como assunto: Europa Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Avaliação da Tecnologia Biomédica / União Europeia / Fortalecimento Institucional / Participação dos Interessados / Política de Saúde Limite: Humans País/Região como assunto: Europa Idioma: En Ano de publicação: 2024 Tipo de documento: Article