Pre-market clinical investigation approval pathways and the role of Early Feasibility Studies for medical devices: a scoping review to guide EU policy.
- DOI
- 10.1080/17434440.2026.2693727
- Published
- 2026 Aug
- Container
- Expert review of medical devices
- Publisher
- Not recorded
- Open access
- unknown
Credibility signals
limited evidence Score 43/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.
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Cite this work
BibTeX
@article{allodium:10.1080/17434440.2026.2693727,
title = {Pre-market clinical investigation approval pathways and the role of Early Feasibility Studies for medical devices: a scoping review to guide EU policy.},
author = {Banks H and Buzelli ML and Tangila Kayembe O and Martelli N and Geraghty M and Callea G},
year = {2026},
journal = {Expert review of medical devices},
doi = {10.1080/17434440.2026.2693727},
url = {https://doi.org/10.1080/17434440.2026.2693727}
}RIS
TY - JOUR TI - Pre-market clinical investigation approval pathways and the role of Early Feasibility Studies for medical devices: a scoping review to guide EU policy. AU - Banks H AU - Buzelli ML AU - Tangila Kayembe O AU - Martelli N AU - Geraghty M AU - Callea G PY - 2026 JO - Expert review of medical devices DO - 10.1080/17434440.2026.2693727 UR - https://doi.org/10.1080/17434440.2026.2693727 ER -
APA
H, B., ML, B., O, T. K., N, M., M, G., & G, C. (2026). Pre-market clinical investigation approval pathways and the role of Early Feasibility Studies for medical devices: a scoping review to guide EU policy.. Expert review of medical devices. https://doi.org/10.1080/17434440.2026.2693727
Source records
- pubmed · retrieved 2026-09-25T21:27:41.613Z