Littérature PubMed
Publications sur les dispositifs médicaux issues de PubMed / NCBI
Analyse des tendances des dispositifs de prothèse de hanche retirés par la FDA : une revue rétrospective
Lire la suite →Cybersecurity breaches in medical devices: analyzing FDA safety communications in response to patient security concerns.
Lire la suite →Un cadre d'indice multidimensionnel pour évaluer l'applicabilité réglementaire de l'ISO 10328 à l'aide d'un cas d'étude de genou prothétique
Lire la suite →Urologic Device Innovation and Trends: An Analysis of Food and Drug Administration Approvals From 1990 to 2023.
Lire la suite →Medical Device Regulation - Who Does the FDA Serve?
Lire la suite →Device failures and patient adverse events from EUS: 26-year FDA MAUDE analysis (2000-2025).
Lire la suite →Artificial intelligence as medical device in radiology in 2025: the regulatory scenario in the EU, USA, and China.
Lire la suite →Clinical Trial Design and Regulatory Requirements for Artificial Intelligence as a Medical Device: A PRISMA-ScR-Guided Scoping Review of Global Guidance and Evidence (2017-2025).
Lire la suite →The history of state preemption and medical device regulation: lessons for artificial intelligence oversight.
Lire la suite →FDA-Regulated AI-Enabled Medical Devices With Pediatric Indications.
Lire la suite →Use and regulation of patient-specific three-dimensional printing in medicine: a survey of physician end-users.
Lire la suite →Aucun article correspondant.
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