Challenges faced by manufacturers with clinical evaluation under the new European Medical Device Regulations
AbstractThis study seeks to investigate the impact of strengthened requirements for clinical evaluation for medical device manufacturers in Europe due to the new Medical Device Regulations. Qualitative interviews were conducted with eight clinical evaluation consultants from eight different European...
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| Principais autores: | , |
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| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Taylor & Francis Group
2023-12-01
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| 叢編: | Cogent Engineering |
| 主題: | |
| 在線閱讀: | https://www.tandfonline.com/doi/10.1080/23311916.2023.2261236 |
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