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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6612978/ https://www.ncbi.nlm.nih.gov/pubmed/31308772 http://dx.doi.org/10.2147/PROM.S212991 |