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Medical Device Regulation: Should We Care About It?
Medical devices are subject to strict regulatory and approval processes to enter the market and to be used by operators and patients. These are needed to guarantee the users’ safety. The different activities of these processes have important implications for all involved stakeholders and for the who...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Springer Netherlands
2022
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8968778/ https://www.ncbi.nlm.nih.gov/pubmed/35378951 http://dx.doi.org/10.1007/s44200-022-00014-0 |