Commentary: Europe needs a central, transparent, and evidence based regulation process for devices
Author:
Publisher
BMJ
Subject
General Engineering
Cited by 32 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Different regulatory framework for medical devices and drugs in the European Union: Impact on clinical research and health technology assessments;The International Journal of Health Planning and Management;2023-06-14
2. After the four-year transition period: Is the European Union's Medical Device Regulation of 2017 likely to achieve its main goals?;Health Policy;2022-12
3. Preparing healthcare, academic institutions, and notified bodies for their involvement in the innovation of medical devices under the new European regulation;Expert Review of Medical Devices;2022-08-03
4. Review of investigational medical devices' clinical trials and regulations in Africa as a benchmark for new innovations;Frontiers in Medical Technology;2022-07-28
5. Exploring the reporting standards of RCTs involving invasive procedures for assisted vaginal birth: A systematic review;European Journal of Obstetrics & Gynecology and Reproductive Biology;2021-07
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