Automated surveillance to detect post-procedure safety signals of approved medical devices

CONTEXT: Assuring the safety of medical devices challenges current surveillance approaches which rely heavily on voluntary reporting of adverse events. Automated surveillance of clinical registries may provide early warnings in the post-market evaluation of medical device safety. OBJECTIVE: To deter...

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Vydáno v:JAMA
Hlavní autoři: Resnic, Frederic S., Gross, Thomas P., Marinac-Dabic, Danica, Loyo-Berrios, Nilsa, Donnelly, Sharon, Normand, Sharon-Lise T., Matheny, Michael E.
Médium: Artigo
Jazyk:Inglês
Vydáno: 2010
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Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5130290/
https://ncbi.nlm.nih.gov/pubmed/21063011
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/jama.2010.1633
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