PubMed-Literatur
Publikationen zu Medizinprodukten aus PubMed / NCBI
Interpreting the two-hour partial REBOA safety window: Physiologic context, monitoring limitations, and device-specific considerations.
Mehr lesen →Digital Mental Health: A Narrative Review of FDA-Authorized Products for Psychiatric Treatment and Diagnostic Support.
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Mehr lesen →Time-series and thematic analyses of clinical utilities and operational issues in early clinical studies of the da Vinci surgical system.
Mehr lesen →Cybersecurity and Privacy Risks of Generative AI Mental-Health Chatbots: A Systematic Review and Regulatory Framework.
Mehr lesen →Towards a feature-based regulatory benchmark for user-centred SaMD design in cancer care.
Mehr lesen →Automating Safety Surveillance for Software-Based Medical Devices: Insights from FDA MAUDE Data.
Mehr lesen →Ethical concerns regarding a lack of standardized clinical demographic data: an audit of 2023 FDA medical devices.
Mehr lesen →Ethical Responsibility in the Off-Label Use of AI in Medical Imaging.
Mehr lesen →Impact1: Supporting Innovation in Pediatric and Maternal Health-5 Years of Outcomes.
Mehr lesen →Global pharmacovigilance reporting: comparative analysis of adverse event obligations across five major regulatory authorities.
Mehr lesen →Keine passenden Artikel.
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