Littérature PubMed
Publications sur les dispositifs médicaux issues de PubMed / NCBI
Interpreting the two-hour partial REBOA safety window: Physiologic context, monitoring limitations, and device-specific considerations.
Lire la suite →Digital Mental Health: A Narrative Review of FDA-Authorized Products for Psychiatric Treatment and Diagnostic Support.
Lire la suite →Un profil minimal de correspondance UDI-DICOM et artefact de validation pour les flux de travail d'imagerie de dispositifs médicaux
Lire la suite →Time-series and thematic analyses of clinical utilities and operational issues in early clinical studies of the da Vinci surgical system.
Lire la suite →Cybersecurity and Privacy Risks of Generative AI Mental-Health Chatbots: A Systematic Review and Regulatory Framework.
Lire la suite →Towards a feature-based regulatory benchmark for user-centred SaMD design in cancer care.
Lire la suite →Automating Safety Surveillance for Software-Based Medical Devices: Insights from FDA MAUDE Data.
Lire la suite →Ethical concerns regarding a lack of standardized clinical demographic data: an audit of 2023 FDA medical devices.
Lire la suite →Ethical Responsibility in the Off-Label Use of AI in Medical Imaging.
Lire la suite →Impact1: Supporting Innovation in Pediatric and Maternal Health-5 Years of Outcomes.
Lire la suite →Global pharmacovigilance reporting: comparative analysis of adverse event obligations across five major regulatory authorities.
Lire la suite →Aucun article correspondant.
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