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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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Podrobná bibliografie
Vydáno v:Patient Relat Outcome Meas
Hlavní autoři: Kavanagh, Kevin T, Brown, Raeford E, Kraman, Steve S, Calderon, Lindsay E, Kavanagh, Sean P
Médium: Artigo
Jazyk:Inglês
Vydáno: Dove 2019
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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