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An Ethical Risk Management Approach for Medical Devices
INTRODUCTION: The Food and Drug Administration (FDA) audits and validates devices before mass production to ensure high standards, safety, and quality of medical devices being marketed. Despite those measures in place, consumers’ trusts in medical devices are still dwindling based on safety and priv...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Dove
2021
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8184284/ https://www.ncbi.nlm.nih.gov/pubmed/34113187 http://dx.doi.org/10.2147/RMHP.S306698 |