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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Bibliographic Details
Main Authors: Petra Maresova, Lukas Rezny, Lukas Peter, Ladislav Hajek, Frank Lefley
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-04-01
Series:Frontiers in Public Health
Subjects:
SME
Online Access:https://www.frontiersin.org/articles/10.3389/fpubh.2021.666453/full