From QSR and ISO 13485 to QMSR: A Review of the U.S. Medical Device Quality Transition and Its Differential Impact on OEMs, Contract Manufacturers, and Critical Component Suppliers
- DOI
- 10.20944/preprints202609.1175.v1
- Published
- 2026-09-15
- Container
- Not recorded
- Publisher
- MDPI AG
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.20944/preprints202609.1175.v1,
title = {From QSR and ISO 13485 to QMSR: A Review of the U.S. Medical Device Quality Transition and Its Differential Impact on OEMs, Contract Manufacturers, and Critical Component Suppliers},
author = {Rahul Kanety},
year = {2026},
doi = {10.20944/preprints202609.1175.v1},
url = {https://doi.org/10.20944/preprints202609.1175.v1}
}RIS
TY - JOUR TI - From QSR and ISO 13485 to QMSR: A Review of the U.S. Medical Device Quality Transition and Its Differential Impact on OEMs, Contract Manufacturers, and Critical Component Suppliers AU - Rahul Kanety PY - 2026 DO - 10.20944/preprints202609.1175.v1 UR - https://doi.org/10.20944/preprints202609.1175.v1 ER -
APA
Kanety, R. (2026). From QSR and ISO 13485 to QMSR: A Review of the U.S. Medical Device Quality Transition and Its Differential Impact on OEMs, Contract Manufacturers, and Critical Component Suppliers. https://doi.org/10.20944/preprints202609.1175.v1
Source records
- crossref · retrieved 2026-09-25T08:44:09.920Z