Литература PubMed
Публикации о медицинских изделиях из PubMed / NCBI
Software as Medical Devices: requirements and regulatory landscape in the United States.
Читать далее →Navigating through regulatory frameworks for digital therapeutics and biomarkers.
Читать далее →Evaluation of a Single Knee System: All-Polyethylene Tibia (APT) vs. Metal-Backed Tibia (MBT) in Primary Total Knee Arthroplasty.
Читать далее →Regulatory Adoption of AI, ML, Computational Modeling & Simulation in In-Silico Clinical Trials for Medical Devices: A Systematic Review.
Читать далее →Artificial intelligence in personalized prescription: A narrative review of promise, peril, and practicality.
Читать далее →Stakeholder Perspectives on Early Feasibility Studies for Digital Health Technologies in the European Union: Qualitative Interview Study.
Читать далее →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).
Читать далее →Competitive value of acquiring novel FDA product codes for medical device manufacturers: an original investigation.
Читать далее →The Essential Role of Medical Monitors in Clinical Trials.
Читать далее →Clearing the airway? A pilot cadaveric study of the LifeVac™ device.
Читать далее →Benefit-Risk Reporting for FDA-Cleared Artificial Intelligence-Enabled Medical Devices.
Читать далее →Подходящих статей не найдено.
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