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An Inclusive Civil Society Dialogue for Successful Implementation of the EU HTA Regulation: Call to Action to Ensure Appropriate Involvement of Stakeholders and Collaborators

  • Thomas Desmet
  • , Elaine Julian
  • , Walter Van Dyck
  • , Isabelle Huys
  • , Steven Simoens
  • , Rosa Giuliani
  • , Mondher Toumi
  • , Christian Dierks
  • , Juliana Dierks
  • , Antonella Cardone
  • , Francois Houÿez
  • , Mira Pavlovic
  • , Michael Berntgen
  • , Peter Mol
  • , Anja Schiel
  • , Wim Goettsch
  • , Fabrizio Gianfrate
  • , Stefano Capri
  • , James Ryan
  • , Pierre Ducournau
  • Oriol Solà-Morales, Jörg Ruof
  • Vlerick Business School
  • Secretariat of the European Access Academy (EAA)
  • University of Padova
  • Guy's and St Thomas' NHS Foundation Trust
  • Aix-Marseille University
  • Dierks+ Company
  • Cancer Patients Europe
  • European Organisation for Rare Diseases (EURORDIS)
  • Medicines Development and Training (MDT) Services
  • European Medicines Agency (EMA)
  • University of Groningen
  • Norwegian Medicines Agency (NOMA)
  • University of Ferrara
  • Cattaneo-LIUC University
  • Astra Zeneca
  • AbbVie
  • International University of Catalonia-UIC

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

OBJECTIVES: Stakeholder involvement has long been considered a success factor for a joint European health technology assessment (HTA) process, and its relevance is now anchored in the EU HTA Regulation's (EU HTAR) legislative wording. Therefore, we aimed to explore the roles, challenges, and most important activities to increase the level of involvement per stakeholder group.

METHODS: At the 2022 Fall Convention of the European Access Academy (EAA), working groups addressed the involvement of patients, clinicians, regulators, health technology developers (HTD), and national HTA bodies and payers within the EU HTA process. Each working group revisited the pre-convention survey results, determined key role characteristics for each stakeholder, and agreed on the most important activities to fulfill the role profile. Finally, the activities suggested per group were prioritized by plenary group.

RESULTS: The prioritized actions for patients included training and capacity building, the establishment of a patient involvement committee, and the establishment of a patient unit at the EC secretariat. For clinicians, it included alignment on evidence assessment from a clinical vs. HTA point of view, capacity building, and standardization of processes. The most important actions for regulators are to develop joint regulatory-HTA guidance documents, align processes and interfaces under the regulation, and share discussions on post-licensing evidence generation. HTDs prioritized scientific advice capacity and the review of the scoping process, and further development of the scope of the assessment report fact checks. The top three actions for national HTA bodies and payers included clarification on the early HTD dialogue process, political support and commitment, and clarification on financial support.

CONCLUSIONS: Addressing the activities identified as the most important for stakeholders/collaborators in the EU HTA process (e.g., in the implementation of the EU HTA Stakeholder Network and of the guidance documents developed by the EUnetHTA 21 consortium) will be key to starting an " inclusive civil society dialogue", as suggested by the European Commission's Pharmaceutical Strategy.

Original languageEnglish
Pages (from-to)21-34
Number of pages14
JournalJournal of market access & health policy
Volume12
Issue number1
DOIs
Publication statusPublished - Mar 2024

Bibliographical note

Publisher Copyright:
© 2024 by the authors.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • EUHTA
  • health policy
  • health technology assessment
  • stakeholder involvement

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