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Priorities for medical device regulatory approval: a report from the European Society of Cardiology Cardiovascular Round Table.

Publication ,  Journal Article
Windecker, S; Fraser, AG; Szymanski, P; Gilard, M; Lüscher, TF; Abid, L; Brennan, J; Byrne, R; Crotti, L; Drossart, I; Franke, J; Cossellu, MG ...
Published in: Eur Heart J
April 22, 2025

The European Union (EU) Medical Device Regulation increased regulatory scrutiny to improve the safety and performance of new medical devices. An equally important goal is providing timely access to innovative devices to benefit patient care. The European Society of Cardiology strongly advocates for the evolution of the Medical Device Regulation system to facilitate priority access for innovative devices for unmet needs and orphan cardiovascular (CV) medical devices in EU countries. Although device approval is currently executed by Notified Bodies in the EU, it will be advantageous in the mid-term to consider a single EU regulatory agency for devices. In the short term, steps can be taken to transform the current system into a more efficient, predictable, cost-effective, and user-friendly service. Key strategies include the following: enhancing predictability of the approval process through use of early scientific advice from regulators; establishing unique regulatory pathways for CV orphan, paediatric, and innovative devices; promoting more efficient (re)certification of essential legacy CV devices; improving transparency of sponsor interactions with Notified Bodies; expanding the roles of the Expert Panels to assist in the approval of CV devices; promoting global regulatory harmonization, considering streamlined authorization of CV medical technologies across selected jurisdictions; developing an efficient system to monitor device safety; and ensuring funding for data collection platforms. Some strategies that could help include considering a pilot programme for joint approval processes of selected devices in partnership with other regions (i.e. US Food and Drug Administration); developing priority pathways for accelerated access to innovative or orphan devices; and increasing recognition of the importance of early feasibility studies in the EU.

Duke Scholars

Published In

Eur Heart J

DOI

EISSN

1522-9645

Publication Date

April 22, 2025

Volume

46

Issue

16

Start / End Page

1469 / 1479

Location

England

Related Subject Headings

  • Societies, Medical
  • Medical Device Legislation
  • Humans
  • European Union
  • Europe
  • Equipment and Supplies
  • Device Approval
  • Cardiovascular System & Hematology
  • Cardiology
  • 3202 Clinical sciences
 

Citation

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Windecker, S., Fraser, A. G., Szymanski, P., Gilard, M., Lüscher, T. F., Abid, L., … Weidinger, F. (2025). Priorities for medical device regulatory approval: a report from the European Society of Cardiology Cardiovascular Round Table. Eur Heart J, 46(16), 1469–1479. https://doi.org/10.1093/eurheartj/ehaf069
Windecker, Stephan, Alan G. Fraser, Piotr Szymanski, Martine Gilard, Thomas F. Lüscher, Leila Abid, John Brennan, et al. “Priorities for medical device regulatory approval: a report from the European Society of Cardiology Cardiovascular Round Table.Eur Heart J 46, no. 16 (April 22, 2025): 1469–79. https://doi.org/10.1093/eurheartj/ehaf069.
Windecker S, Fraser AG, Szymanski P, Gilard M, Lüscher TF, Abid L, et al. Priorities for medical device regulatory approval: a report from the European Society of Cardiology Cardiovascular Round Table. Eur Heart J. 2025 Apr 22;46(16):1469–79.
Windecker, Stephan, et al. “Priorities for medical device regulatory approval: a report from the European Society of Cardiology Cardiovascular Round Table.Eur Heart J, vol. 46, no. 16, Apr. 2025, pp. 1469–79. Pubmed, doi:10.1093/eurheartj/ehaf069.
Windecker S, Fraser AG, Szymanski P, Gilard M, Lüscher TF, Abid L, Brennan J, Byrne R, Crotti L, Drossart I, Franke J, Cossellu MG, Kirtane AJ, Kurucova J, Krucoff M, McGauran G, Myers PO, O’Connor DB, Parma R, Piscoi P, Rao A, Rappagliosi A, Stefanini G, Samset E, Vincent A, von Bardeleben RS, Weidinger F. Priorities for medical device regulatory approval: a report from the European Society of Cardiology Cardiovascular Round Table. Eur Heart J. 2025 Apr 22;46(16):1469–1479.
Journal cover image

Published In

Eur Heart J

DOI

EISSN

1522-9645

Publication Date

April 22, 2025

Volume

46

Issue

16

Start / End Page

1469 / 1479

Location

England

Related Subject Headings

  • Societies, Medical
  • Medical Device Legislation
  • Humans
  • European Union
  • Europe
  • Equipment and Supplies
  • Device Approval
  • Cardiovascular System & Hematology
  • Cardiology
  • 3202 Clinical sciences