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Reporter’s occupation and source of adverse device event reports contained in the FDA’s MAUDE database
INTRODUCTION: A review of the medical device adverse events submitted to the United States Food & Drug Administration (FDA) Manufacturer and User Facility Device Experience (MAUDE) database was undertaken to determine the major sources of the information. METHODS: The reporter’s occupation and s...
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| Vydáno v: | Patient Relat Outcome Meas |
|---|---|
| Hlavní autoři: | , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Dove
2019
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6612978/ https://ncbi.nlm.nih.gov/pubmed/31308772 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/PROM.S212991 |
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