Literatura do PubMed
Publicações sobre dispositivos médicos do PubMed / NCBI
Regulatory Insights From 27 Years of Artificial Intelligence/Machine Learning-Enabled Medical Device Recalls in the United States: Implications for Future Governance.
Ler mais →Clinical trial design in FDA submissions for neuromodulation devices, 1960-2023: a systematic review and meta-analysis.
Ler mais →Assessing the Impact of End-of-Life Processing on Reusable Medical Devices.
Ler mais →The illusion of safety: A report to the FDA on AI healthcare product approvals.
Ler mais →[Regulatory requirements for software medical devices: Comparison between Europe, the United States, and Algeria].
Ler mais →Scoping review on regulation, implementation and postmarket surveillance of medical devices.
Ler mais →Evaluation of clinical data and regulatory submission characteristics for neuromodulation devices approved via the 510(k) pathway (1996-2024).
Ler mais →Um resumo abrangente da evidência real-world na aprovação de dispositivos médicos nos Estados Unidos.
Ler mais →Prescription Digital Therapeutics Research Across Clinical, Engagement, Regulatory, and Implementation Domains: A Bibliometric and Thematic Study.
Ler mais →Decoding FDA Labeling of Prescription Digital Therapeutics: A Cross-Sectional Regulatory Study.
Ler mais →Precisão e Segurança de um Monitor Contínuo de Pressão Arterial Não Invasiva em Neonatos
Ler mais →Nenhum artigo correspondente.
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