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Barriers to medical device innovation
The US Food and Drug Administration (FDA) has defined a medical device as a health care product that does not achieve it’s purpose by chemical action or by being metabolized. This means that a vast number of products are considered medical devices. Such devices play an essential role in the practice...
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Autors principals: | , , |
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Format: | Artigo |
Idioma: | Inglês |
Publicat: |
Dove Medical Press
2014
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Matèries: | |
Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4063798/ https://ncbi.nlm.nih.gov/pubmed/24966699 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/MDER.S43369 |
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