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
| Autor: | Rosanna Tarricone, Helen Banks, Oriana Ciani, Werner Brouwer, Michael F Drummond, Reiner Leidl, Nicolas Martelli, Laura Sampietro-Colom, Rod S. Taylor |
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| Přispěvatelé: | Health Economics (HE) |
| Jazyk: | angličtina |
| Rok vydání: | 2023 |
| Předmět: |
INNOVATIVE MEDICAL DEVICES
CLINICAL EVIDENCE SURROGATE ENDPOINT Biomedical Engineering HIGH-RISK IMPLANTABLE MEDICAL DEVICES EARLY DIALOGUE ACCELERATED APPROVAL General Medicine COVERAGE ACCELERATED APPROVAL EUROPEAN UNION HTA REGULATION CLINICAL EVIDENCE COVERAGE EARLY DIALOGUE HIGH-RISK IMPLANTABLE MEDICAL DEVICES INNOVATIVE MEDICAL DEVICES MEDICAL DEVICE REGULATION SURROGATE ENDPOINT HTA REGULATION MEDICAL DEVICE REGULATION Surgery EUROPEAN UNION |
| Zdroj: | Expert Review of Medical Devices, 20(4), 259-271. Taylor & Francis Ltd |
| ISSN: | 1743-4440 |
| Popis: | 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. |
| Databáze: | OpenAIRE |
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