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

• 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.
• 主題: article
• オンライン･アクセス: Connect to this object online.

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...