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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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:JAMA
Päätekijät: Resnic, Frederic S., Gross, Thomas P., Marinac-Dabic, Danica, Loyo-Berrios, Nilsa, Donnelly, Sharon, Normand, Sharon-Lise T., Matheny, Michael E.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2010
Aiheet:
Linkit: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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