Medical Device Safety Throughout the Product Lifecycle: Regulatory Frameworks, Digital Transformation, and the Role of Artificial Intelligence in Devices and Monitoring.
- DOI
- 10.1016/j.clinthera.2026.08.013
- Published
- 2026 Sep 16
- Container
- Clinical therapeutics
- Publisher
- Not recorded
- Open access
- no
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Cite this work
BibTeX
@article{allodium:10.1016/j.clinthera.2026.08.013,
title = {Medical Device Safety Throughout the Product Lifecycle: Regulatory Frameworks, Digital Transformation, and the Role of Artificial Intelligence in Devices and Monitoring.},
author = {Vaezzadeh S and Oyesile C and Barber N and Pakkal B},
year = {2026},
journal = {Clinical therapeutics},
doi = {10.1016/j.clinthera.2026.08.013},
url = {https://doi.org/10.1016/j.clinthera.2026.08.013}
}RIS
TY - JOUR TI - Medical Device Safety Throughout the Product Lifecycle: Regulatory Frameworks, Digital Transformation, and the Role of Artificial Intelligence in Devices and Monitoring. AU - Vaezzadeh S AU - Oyesile C AU - Barber N AU - Pakkal B PY - 2026 JO - Clinical therapeutics DO - 10.1016/j.clinthera.2026.08.013 UR - https://doi.org/10.1016/j.clinthera.2026.08.013 ER -
APA
S, V., C, O., N, B., & B, P. (2026). Medical Device Safety Throughout the Product Lifecycle: Regulatory Frameworks, Digital Transformation, and the Role of Artificial Intelligence in Devices and Monitoring.. Clinical therapeutics. https://doi.org/10.1016/j.clinthera.2026.08.013
Source records
- pubmed · retrieved 2026-09-25T16:32:38.222Z
- europe-pmc · retrieved 2026-09-25T16:32:38.239Z