Littérature PubMed
Publications sur les dispositifs médicaux issues de PubMed / NCBI
Innovation trajectory of Software as a Medical Device: Evidence from the US FDA-approved products.
Lire la suite →Pre-market clinical investigation approval pathways and the role of Early Feasibility Studies for medical devices: a scoping review to guide EU policy.
Lire la suite →Radiation Oncology Device Recalls (2015-2025): Software and Artificial Intelligence as Emerging Drivers of Postmarket Safety.
Lire la suite →Patient Preference Information (PPI) in Medical Device Development: A Cross-Industry Review of Use-Cases.
Lire la suite →Regulating digital surgery to balance safety and innovation: a SAGES white paper.
Lire la suite →Two decades of growth and trends in the FDA authorization of digital medical devices.
Lire la suite →Artificial intelligence in urology: A review of United States Food and Drug Administration-cleared devices.
Lire la suite →Borrowing from the cancer playbook: a master protocol basket trial for hard-to-heal wound therapeutics targeting shared pathobiology.
Lire la suite →Une Histoire de la Réglementation des Dispositifs Médicaux aux États-Unis et le Cadre Réglementaire Actuel.
Lire la suite →Reliability and Consistency Analysis of Multiple Instruments for Scoliosis Screening in Adolescent Males: A Comparative Study of Instrument Accuracy.
Lire la suite →Regulatory science for AI-based software as a medical device in computational pathology and biomarker-driven drug development.
Lire la suite →Aucun article correspondant.
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