EU postmarket surveillance plans for medical devices

PURPOSE: Recent public health safety issues involving medical devices have led to a growing demand to improve the current passive‐reactive postmarket surveillance (PMS) system. Various European Union (EU) national competent authorities have started to focus on strengthening the postmarket risk evalu...

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Detalles Bibliográficos
Autores principales: Pane, Josep, Francisca, Reynold D.C., Verhamme, Katia M.C., Orozco, Marcia, Viroux, Hilde, Rebollo, Irene, Sturkenboom, Miriam C.J.M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6771951/
https://www.ncbi.nlm.nih.gov/pubmed/31318470
http://dx.doi.org/10.1002/pds.4859

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6771951/
https://www.ncbi.nlm.nih.gov/pubmed/31318470
http://dx.doi.org/10.1002/pds.4859

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