ORCID: https://orcid.org/0000-0002-2009-9357; Banks, Helen
ORCID: https://orcid.org/0000-0003-0337-1715; Ciani, Oriana
ORCID: https://orcid.org/0000-0002-3607-0508; Brouwer, Werner
ORCID: https://orcid.org/0000-0002-0476-8397; Drummond, Michael F
ORCID: https://orcid.org/0000-0002-6968-4610; Leidl, Reiner
ORCID: https://orcid.org/0000-0002-7115-7510; Martelli, Nicolas
ORCID: https://orcid.org/0000-0001-5959-231X; Sampietro-Colom, Laura
ORCID: https://orcid.org/0000-0001-7182-0231 und Taylor, Rod S.
ORCID: https://orcid.org/0000-0002-3043-6011
(3. April 2023):
An accelerated access pathway for innovative high-risk medical devices under the new European Union Medical Devices and health technology assessment regulations? Analysis and recommendations.
In: Expert Review of Medical Devices, Bd. 20, Nr. 4: S. 259-271
[PDF, 2MB]

Abstract
Introduction: The new European Union (EU) Regulations for medical devices (MDs) and health technology assessment (HTA) are welcome developments that should increase the quality of clinical evidence for MDs and reduce fragmentation in the EU market access process. To fully exploit anticipated benefits, their respective assessment processes should be closely coordinated, particularly for promising, highly innovative MDs. Accelerated approval is worth exploring for certain categories of high-risk MDs to keep the EU regulatory process competitive compared to accelerated MD approval programs elsewhere (e.g. US).
Areas covered: Problems observed in worldwide accelerated drug and MD regulatory approval programs are reviewed, including greater uncertainty in premarket clinical evidence generation and lack of oversight for post approval evidence requirements. Implications for MD approval, HTA and coverage are explored.
Expert opinion: Through analysis of two decades of drug and MD accelerated approval programs worldwide, recommendations for an Accelerated Access Pathway for select innovative, high-risk MDs are proposed to fit the EU context, leverage the two new regulations, increase opportunities for Expert Panels to provide timely advice regarding manufacturers' evidence generation plans along the MD lifecycle (pre, postmarket), and safely speed patient access while promoting increased collaboration among Member States on coverage decisions.
Dokumententyp: | Zeitschriftenartikel |
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Fakultät: | Betriebswirtschaft > Institut für Gesundheitsökonomie und Management im Gesundheitswesen |
Themengebiete: | 300 Sozialwissenschaften > 330 Wirtschaft
600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin und Gesundheit |
URN: | urn:nbn:de:bvb:19-epub-125669-8 |
ISSN: | 1743-4440 |
Sprache: | Englisch |
Dokumenten ID: | 125669 |
Datum der Veröffentlichung auf Open Access LMU: | 19. Mai 2025 08:29 |
Letzte Änderungen: | 19. Mai 2025 08:29 |