Littérature PubMed
Publications sur les dispositifs médicaux issues de PubMed / NCBI
Post-marketing surveillance framework of cell and gene therapy products in the European Union, the United States, Japan, South Korea and China: a comparative study.
Lire la suite →Medical device similarity analysis: a promising approach to medical device equivalence regulation.
Lire la suite →Class I Recalls of Cardiovascular Devices Between 2013 and 2022 : A Cross-Sectional Analysis.
Lire la suite →Regulatory Aspects of Artificial Intelligence and Machine Learning.
Lire la suite →Evaluating Medical Devices in Nephrology Using Patient-Reported Outcome and Experience Measures.
Lire la suite →Requirements to bring a medical device to market.
Lire la suite →Harmonization of regulatory frameworks for medical devices in BRICS countries: A path to enhanced trade and investment.
Lire la suite →Lessons on the use of real-world data in medical device research: findings from the National Evaluation System for Health Technology Test-Cases.
Lire la suite →Recent Advances in the Design and Application of Shoulder Arthroplasty Implant Systems and Their Impact on Clinical Outcomes: A Comprehensive Review.
Lire la suite →Validation analytique du test des acides ribonucléiques fécaux multitarget pour le dépistage du cancer colorectal.
Lire la suite →Regulating AI-Based Medical Devices in Saudi Arabia: New Legal Paradigms in an Evolving Global Legal Order.
Lire la suite →Aucun article correspondant.
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