After the four-year transition period: Is the European Union's Medical Device Regulation of 2017 likely to achieve its main goals?-Reference-Cited by-同舟云学术

After the four-year transition period: Is the European Union's Medical Device Regulation of 2017 likely to achieve its main goals?

Published:2022-12 Issue:12 Volume:126 Page:1233-1240
ISSN:0168-8510
Container-title:Health Policy
language:en
Short-container-title:Health Policy

Author:

Shatrov Kosta^ORCID,Blankart Carl Rudolf^ORCID

Publisher

Elsevier BV

Subject

Health Policy

Reference54 articles.

1. European Commission's Official Website. Internal Market, Industry, Entrepreneurship and SMEs: medical Devices. [January 07, 2020]; Available from: https://ec.europa.eu/growth/sectors/medical-devices.

2. Medicines and Healthcare products Regulatory Agency. A summary of the evidence on the benefits and risks of vaginal mesh implants. 2022.

3. Ongoing problems with metal-on-metal hip implants;Heneghan;BMJ,2012

4. The Poly Implant Prothèse breast prostheses scandal: embodied risk and social suffering;Greco;Soc Sci Med,2015

5. A structured approach for investigating the causes of medical device adverse events;Amoore;J Med Eng,2014

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