Do Regulatory Changes Seriously Affect the Medical Devices Industry? Evidence From the Czech Republic

Background: Within the EU, some of the challenges and perceived risks now facing medical device (MD) developers result from changes in the regulatory framework, emphasizing safety. Therefore, medical technology companies must adopt stricter quality assurance measures so that individual devices can b...

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Detalles Bibliográficos
Autores principales: Maresova, Petra, Rezny, Lukas, Peter, Lukas, Hajek, Ladislav, Lefley, Frank
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Public Health
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8113379/
https://www.ncbi.nlm.nih.gov/pubmed/33996732
http://dx.doi.org/10.3389/fpubh.2021.666453

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8113379/
https://www.ncbi.nlm.nih.gov/pubmed/33996732
http://dx.doi.org/10.3389/fpubh.2021.666453

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