Littérature PubMed
Publications sur les dispositifs médicaux issues de PubMed / NCBI
Systematic review of usability evaluations in medical devices: Methodological choices, heuristic application, and confounding factors.
Lire la suite →Regulatory Landscape of Regenerative Dermatology: Current Frameworks and Future.
Lire la suite →US FDA approves home-delivered tDCS for treating depression.
Lire la suite →Is the current regulatory framework for direct-to-consumer microbiome-based tests sufficient to protect consumers from medical, economic, and dignitary harms?
Lire la suite →Clinical Evidence to Support US Food and Drug Administration Review of New Medical Technology in Pulmonary, Sleep, and Critical Care Medicine Between 2014 and 2024: A Scoping Review to Support Adoption in Practice.
Lire la suite →Evaluating commercial multimodal AI for diabetic eye screening and implications for an alternative regulatory pathway.
Lire la suite →Characterization and Time-delay in Issuing High-risk Recalls of Orthopaedic Devices From 2002 to 2023.
Lire la suite →Machine Learning-Enabled Medical Devices Authorized by the US Food and Drug Administration in 2024: Regulatory Characteristics, Predicate Lineage, and Transparency Reporting.
Lire la suite →Few FDA Approved AI/ML Orthopaedic Devices Have EU MDR Equivalents or Peer-Reviewed Validation.
Lire la suite →Describing Inconsistencies in Pediatric Labeling of Medical Devices.
Lire la suite →[Regulatory Practices and Implications of FDA Approving New Drug Indication under the Medical Device Pathway].
Lire la suite →Aucun article correspondant.
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