PubMed-Literatur
Publikationen zu Medizinprodukten aus PubMed / NCBI
Genehmigung und Zertifizierung von ophthalmischen AI-Geräten in der Europäischen Union.
Mehr lesen →Integrating real-world data to assess cardiac ablation device outcomes in a multicenter study using the OMOP common data model for regulatory decisions: implementation and evaluation.
Mehr lesen →Association Between Regulatory Submission Characteristics and Recalls of Medical Devices Receiving 510(k) Clearance.
Mehr lesen →Use of Recalled Devices in New Device Authorizations Under the US Food and Drug Administration's 510(k) Pathway and Risk of Subsequent Recalls.
Mehr lesen →Stakeholder perspectives on scaling up medical device reprocessing: A qualitative study.
Mehr lesen →Why did the number of US FDA medical device guidelines begin to rise in the mid-2010s? A perspective.
Mehr lesen →Diversity in Orthopaedic Surgery Medical Device Clinical Trials: An Analysis of the Food and Drug Administration Safety and Innovation Act.
Mehr lesen →The Value of Scientific Publications in Surgical Device Innovation.
Mehr lesen →ScanMedicine: An online search system for medical innovation.
Mehr lesen →Artificial Intelligence in Breast Cancer Screening: Evaluation of FDA Device Regulation and Future Recommendations.
Mehr lesen →Recommendations for inversion table therapy.
Mehr lesen →Keine passenden Artikel.
Seite 21 von 42