Littérature PubMed
Publications sur les dispositifs médicaux issues de PubMed / NCBI
Regulatory Insights From 27 Years of Artificial Intelligence/Machine Learning-Enabled Medical Device Recalls in the United States: Implications for Future Governance.
Lire la suite →Clinical trial design in FDA submissions for neuromodulation devices, 1960-2023: a systematic review and meta-analysis.
Lire la suite →Assessing the Impact of End-of-Life Processing on Reusable Medical Devices.
Lire la suite →The illusion of safety: A report to the FDA on AI healthcare product approvals.
Lire la suite →[Regulatory requirements for software medical devices: Comparison between Europe, the United States, and Algeria].
Lire la suite →Scoping review on regulation, implementation and postmarket surveillance of medical devices.
Lire la suite →Evaluation of clinical data and regulatory submission characteristics for neuromodulation devices approved via the 510(k) pathway (1996-2024).
Lire la suite →Un aperçu complet de la preuve réelle dans les approbations des dispositifs médicaux aux États-Unis.
Lire la suite →Prescription Digital Therapeutics Research Across Clinical, Engagement, Regulatory, and Implementation Domains: A Bibliometric and Thematic Study.
Lire la suite →Decoding FDA Labeling of Prescription Digital Therapeutics: A Cross-Sectional Regulatory Study.
Lire la suite →Exactitude et sécurité d'un moniteur de pression artérielle continue non invasif chez les nouveau-nés.
Lire la suite →Aucun article correspondant.
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