Littérature PubMed
Publications sur les dispositifs médicaux issues de PubMed / NCBI
Late adverse event reporting from medical device manufacturers to the US Food and Drug Administration: cross sectional study.
Lire la suite →Biosensors in wearable medical devices: Regulatory framework and compliance across US, EU, and Indian markets.
Lire la suite →Characterization of Spine Implant Device Recalls: A 21-Year Analysis.
Lire la suite →Potential health benefits of lactoferrin and derived peptides - how to qualify as a medical device?
Lire la suite →Bridging the Gap in FDA Approval for Pediatric Neuromodulation Devices.
Lire la suite →Ensuring Medical Device Safety: The Role of Standards Organizations and Regulatory Bodies.
Lire la suite →Evaluation of reporting trends in the MAUDE Database: 1991 to 2022.
Lire la suite →Evaluating the Safety and Usability of an Over-the-Counter Medical Device for Adults With Mild to Moderate Hearing Loss: Formative and Summative Usability Testing.
Lire la suite →Navigating Medical Device Product Liability in Obstetrics and Gynecology.
Lire la suite →Could one strategy fit all? A comparison of regulatory guidance from China, Europe, and the USA on medical device clinical evaluation throughout the total product lifecycle.
Lire la suite →Physician-Patient Communication about Novel Drugs and High-Risk Medical Devices.
Lire la suite →Aucun article correspondant.
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