A Primer to the Structure, Content and Linkage of the FDA’s Manufacturer and User Facility Device Experience (MAUDE) Files

INTRODUCTION AND BACKGROUND: The US Food and Drug Administration (FDA)’s Manufacturer and User Facility Device Experience (MAUDE) database is a publicly available resource providing over 4 million records relating to medical device safety. Using downloadable MAUDE files avoids limitations of the onl...

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Detalles Bibliográficos
Autores principales: Ensign, Lisa Garnsey, Cohen, K. Bretonnel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ubiquity Press 2017
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5994953/
https://www.ncbi.nlm.nih.gov/pubmed/29930960
http://dx.doi.org/10.5334/egems.221

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5994953/
https://www.ncbi.nlm.nih.gov/pubmed/29930960
http://dx.doi.org/10.5334/egems.221

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