PubMed-Literatur
Publikationen zu Medizinprodukten aus PubMed / NCBI
Systematic review of usability evaluations in medical devices: Methodological choices, heuristic application, and confounding factors.
Mehr lesen →Regulatory Landscape of Regenerative Dermatology: Current Frameworks and Future.
Mehr lesen →US FDA genehmigt häusliche Lieferung von tDCS zur Behandlung von Depressionen.
Mehr lesen →Is the current regulatory framework for direct-to-consumer microbiome-based tests sufficient to protect consumers from medical, economic, and dignitary harms?
Mehr lesen →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.
Mehr lesen →Evaluating commercial multimodal AI for diabetic eye screening and implications for an alternative regulatory pathway.
Mehr lesen →Characterization and Time-delay in Issuing High-risk Recalls of Orthopaedic Devices From 2002 to 2023.
Mehr lesen →Machine Learning-Enabled Medical Devices Authorized by the US Food and Drug Administration in 2024: Regulatory Characteristics, Predicate Lineage, and Transparency Reporting.
Mehr lesen →Few FDA Approved AI/ML Orthopaedic Devices Have EU MDR Equivalents or Peer-Reviewed Validation.
Mehr lesen →Describing Inconsistencies in Pediatric Labeling of Medical Devices.
Mehr lesen →[Regulatory Practices and Implications of FDA Approving New Drug Indication under the Medical Device Pathway].
Mehr lesen →Keine passenden Artikel.
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