Analysis of the renewed European Medical Device Regulations in the frame of the non – EU regulatory landscape during the COVID facilitated change-Reference-Cited by-同舟云学术

Analysis of the renewed European Medical Device Regulations in the frame of the non – EU regulatory landscape during the COVID facilitated change

Published:2022-10 Issue:10 Volume:111 Page:2674-2686
ISSN:0022-3549
Container-title:Journal of Pharmaceutical Sciences
language:en
Short-container-title:Journal of Pharmaceutical Sciences

Author:

Kanti S P Yamini^ORCID,Csóka Ildikó^ORCID,Adalbert Lívia,Jójárt-Laczkovich Orsolya^ORCID

Publisher

Elsevier BV

Subject

Pharmaceutical Science

Reference63 articles.

1. European Commission, “European Commission- Medical Devices- Sector,” European Commission. https://ec.europa.eu/health/md_sector/overview_en. (accessed Nov. 29, 2021).

2. European Medicine Agency, “Human Regulatory - Medical Devices,” European Medicine Agency. https://www.ema.europa.eu/en/human-regulatory/overview/medical-devices. (accessed Nov. 29, 2021).

3. European Commission, “Internal Market, Industry, Entrepreneurship and SMEs,” European Commission. https://ec.europa.eu/growth/single-market/european-standards/harmonised-standards/medical-devices_en. (accessed Nov. 29, 2021).

4. European Commission, “Medical Devices - New Regulations,” European Commission. https://ec.europa.eu/health/md_newregulations/getting_ready. (accessed Nov. 30, 2021).

5. European Commission, “Medical Devices - EUDAMED,” European Commission. https://ec.europa.eu/health/md_eudamed/overview_en (accessed Nov. 29, 2021).

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