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Barriers to medical device innovation

The US Food and Drug Administration (FDA) has defined a medical device as a health care product that does not achieve it’s purpose by chemical action or by being metabolized. This means that a vast number of products are considered medical devices. Such devices play an essential role in the practice...

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Detalles Bibliográficos
Autores principales: Bergsland, Jacob, Elle, Ole Jakob, Fosse, Erik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4063798/
https://www.ncbi.nlm.nih.gov/pubmed/24966699
http://dx.doi.org/10.2147/MDER.S43369