Reforming medical device regulation in Europe: centralization, governance, and the case for an EU medical device agency
- DOI
- 10.1016/j.lanepe.2026.101908
- Published
- 2027-01
- Container
- The Lancet Regional Health - Europe
- Publisher
- Elsevier BV
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1016/j.lanepe.2026.101908,
title = {Reforming medical device regulation in Europe: centralization, governance, and the case for an EU medical device agency},
author = {Anett Schönfelder and Tom Melvin and Timo Minssen and Stephen Gilbert},
year = {2027},
journal = {The Lancet Regional Health - Europe},
doi = {10.1016/j.lanepe.2026.101908},
url = {https://doi.org/10.1016/j.lanepe.2026.101908}
}RIS
TY - JOUR TI - Reforming medical device regulation in Europe: centralization, governance, and the case for an EU medical device agency AU - Anett Schönfelder AU - Tom Melvin AU - Timo Minssen AU - Stephen Gilbert PY - 2027 JO - The Lancet Regional Health - Europe DO - 10.1016/j.lanepe.2026.101908 UR - https://doi.org/10.1016/j.lanepe.2026.101908 ER -
APA
Schönfelder, A., Melvin, T., Minssen, T., & Gilbert, S. (2027). Reforming medical device regulation in Europe: centralization, governance, and the case for an EU medical device agency. The Lancet Regional Health - Europe. https://doi.org/10.1016/j.lanepe.2026.101908
Source records
- crossref · retrieved 2026-11-07T07:58:17.059Z