Post-market clinical research conducted by medical device manufacturers: a cross-sectional survey

BACKGROUND: In the US, once a medical device is made available for use, several requirements have been established by the US Food and Drug Administration (FDA) to ensure ongoing post-market surveillance of device safety and effectiveness. Our objective was to determine how commonly medical device ma...

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Detalles Bibliográficos
Autores principales: Ross, Joseph S, Blount, Katrina L, Ritchie, Jessica D, Hodshon, Beth, Krumholz, Harlan M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4454210/
https://www.ncbi.nlm.nih.gov/pubmed/26060416
http://dx.doi.org/10.2147/MDER.S82964

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4454210/
https://www.ncbi.nlm.nih.gov/pubmed/26060416
http://dx.doi.org/10.2147/MDER.S82964

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