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Post-market clinical research conducted by medical device manufacturers: a cross-sectional survey
BACKGROUND: In the US, once a medical device is made available for use, several requirements have been established by the US Food and Drug Administration (FDA) to ensure ongoing post-market surveillance of device safety and effectiveness. Our objective was to determine how commonly medical device ma...
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| Publicat a: | Med Devices (Auckl) |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Dove Medical Press
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4454210/ https://ncbi.nlm.nih.gov/pubmed/26060416 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/MDER.S82964 |
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