Clinical evaluation requirements under the new European Union medical device regulation

Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 was published to regulate medical devices with the aim of bolstering the safety, quality, and efficacy of medical products in Europe.1 The regulation covers medical products intended for the diagnosis and treatmen...

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Bibliographic Details
Main Author: Gloria Hernández Hernández
Format: Article
Language:English
Published: Permanyer 2024-11-01
Series:REC: Interventional Cardiology (English Ed.)
Online Access:https://recintervcardiol.org/en/index.php?option=com_content&view=article&id=1289
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