Littérature PubMed
Publications sur les dispositifs médicaux issues de PubMed / NCBI
Software as Medical Devices: requirements and regulatory landscape in the United States.
Lire la suite →Navigating through regulatory frameworks for digital therapeutics and biomarkers.
Lire la suite →Evaluation of a Single Knee System: All-Polyethylene Tibia (APT) vs. Metal-Backed Tibia (MBT) in Primary Total Knee Arthroplasty.
Lire la suite →Regulatory Adoption of AI, ML, Computational Modeling & Simulation in In-Silico Clinical Trials for Medical Devices: A Systematic Review.
Lire la suite →Artificial intelligence in personalized prescription: A narrative review of promise, peril, and practicality.
Lire la suite →Stakeholder Perspectives on Early Feasibility Studies for Digital Health Technologies in the European Union: Qualitative Interview Study.
Lire la suite →Recalls of Arthroscopic Equipment After Food and Drug Administration 510(k) Approval: A Twenty-Year Analysis of Causes, Trends, and Time to Recall (2004 to 2024).
Lire la suite →Competitive value of acquiring novel FDA product codes for medical device manufacturers: an original investigation.
Lire la suite →The Essential Role of Medical Monitors in Clinical Trials.
Lire la suite →Clearing the airway? A pilot cadaveric study of the LifeVac™ device.
Lire la suite →Benefit-Risk Reporting for FDA-Cleared Artificial Intelligence-Enabled Medical Devices.
Lire la suite →Aucun article correspondant.
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