PubMed Literature
Medical device publications from PubMed / NCBI
Clinical trial design in FDA submissions for neuromodulation devices, 1960-2023: a systematic review and meta-analysis.
Read More →Assessing the Impact of End-of-Life Processing on Reusable Medical Devices.
Read More →The illusion of safety: A report to the FDA on AI healthcare product approvals.
Read More →[Regulatory requirements for software medical devices: Comparison between Europe, the United States, and Algeria].
Read More →Development and Commercialization Pathways of AI Medical Devices in the United States: Implications for Safety and Regulatory Oversight.
Read More →Scoping review on regulation, implementation and postmarket surveillance of medical devices.
Read More →Evaluation of clinical data and regulatory submission characteristics for neuromodulation devices approved via the 510(k) pathway (1996-2024).
Read More →A comprehensive overview of real-world evidence in medical device approvals in the United States.
Read More →Prescription Digital Therapeutics Research Across Clinical, Engagement, Regulatory, and Implementation Domains: A Bibliometric and Thematic Study.
Read More →Decoding FDA Labeling of Prescription Digital Therapeutics: A Cross-Sectional Regulatory Study.
Read More →Accuracy and Safety of a Continuous Noninvasive Blood Pressure Monitor in Neonates.
Read More →No matching articles.
Page 12 of 43
Advertisement