A new platform for post-marketing surveillance and real-world evidence data collection for substance-based medical devices

The recent passage of European Union (EU) Regulation 2017/745 on medical devices (MDs) has improved the classification of MDs and revised their approval process and the post-marketing evaluation of their safety and effectiveness, promoting transparency and post-marketing oversight in Europe. This ne...

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主要な著者: Roberto Cioeta (著者), Andrea Cossu (著者), Emiliano Giovagnoni (著者), Marta Rigoni (著者), Paola Muti (著者)
フォーマット: 図書
出版事項: Frontiers Media S.A., 2022-12-01T00:00:00Z.
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3rd Floor Main Library

予約・返却請求 3rd Floor Main Library
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