The EU's system for regulating medical 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. Mapping the development process of transcutaneous neuromuscular electrical stimulation devices for neurorehabilitation, the associated barriers and facilitators, and its applicability to acquired dysarthria: a qualitative study of manufacturers’ perspectives;Disability and Rehabilitation: Assistive Technology;2023-10-19
2. High-resolution vat-photopolymerization of personalized bioceramic implants: new advances, regulatory hurdles, and key recommendations;International Materials Reviews;2023-03-31
3. 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
4. The need for action by evaluators and decision makers in Europe to ensure safe use of medical software;Frontiers in Medical Technology;2022-11-29
5. Implementation of the new EUR IVD regulation and relation with ISO15189 accreditation: Guidance is urgently required for haemostasis testing;International Journal of Laboratory Hematology;2022-09
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