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Reporting of Death in US Food and Drug Administration Medical Device Adverse Event Reports in Categories Other Than Death
IMPORTANCE: In the US, most postmarket medical device safety data are obtained through adverse event reports that are submitted to the US Food and Drug Administration (FDA)’s Manufacturer and User Facility Device Experience (MAUDE) database. Adverse event reports are classified by the reporter as in...
Tallennettuna:
| Julkaisussa: | JAMA Intern Med |
|---|---|
| Päätekijät: | , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
American Medical Association
2021
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8314174/ https://ncbi.nlm.nih.gov/pubmed/34309624 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/jamainternmed.2021.3942 |
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