Medical Device Regulation and current challenges for the implementation of new technologies

Medical Device Regulation and current challenges for the implementation of new technologies

The European Parliament and the European Council on May 26, 2017 decided to introduce the new regulatory framework for medical devices. The transitional period of the so called Medical Device Regulation (EU 2017/745, MDR) should end on May 26, 2020. Currently the European Commission is working on a...

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Autores principales: Kaule Sebastian, Bock Andrea, Dierke Ariane, Siewert Stefan, Schmitz Klaus-Peter, Stiehm Michael, Klar Ernst, Leuchter Matthias, Lenarz Thomas, Zygmunt Marek, Schmidt Wolfram, Grabow Niels
Formato: article
Lenguaje:EN
Publicado: De Gruyter 2020
Materias:
medical device regulation
ce-certification
regulatory affairs
Medicine
R
Acceso en línea:https://doaj.org/article/6e80e29241a24717ab6126b0ade16be1
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https://doaj.org/article/6e80e29241a24717ab6126b0ade16be1

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