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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| Main Author: | |
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| Format: | Article |
| Language: | English |
| Published: |
Permanyer
2024-11-01
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| 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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