PubMed Literature
Medical device publications from PubMed / NCBI
Medical Device Safety Throughout the Product Lifecycle: Regulatory Frameworks, Digital Transformation, and the Role of Artificial Intelligence in Devices and Monitoring.
Read More →Lean-Agile Product Development in FDA Relevant and Regulated Medical Device Contexts.
Read More →Regulating cell and xeno-transplants: Learning from medical device oversight.
Read More →Artificial Intelligence in Indian Dermatology: An IADVL Academy Position Statement and Policy Framework for Safe, Equitable, and Effective Adoption.
Read More →Networked Radiology Imaging and Treatment Planning Systems and FDA Cybersecurity Regulation: A Difference-in-Differences Analysis of 510(k) Clearance Delays.
Read More →Sensitivity of 510(k) medical device filings to government shutdowns: a brief communication.
Read More →Public transparency and physicochemical standardization in the regulation of PMMA dermal fillers: a comparative analysis of FDA, EU MDR, and ANVISA frameworks.
Read More →Clinical Specialty Expansion of AI-Enabled and Machine Learning-Enabled Medical Devices Authorized by the US Food and Drug Administration From 1995 to 2025: Longitudinal Content Analysis.
Read More →Deployer-side governance of medical imaging artificial intelligence: the regulatory readiness instrument (RRI-MI) for multi-jurisdictional and post-market compliance.
Read More →Bridging Early Feasibility and Pivotal Trials: Insights From Transcatheter Tricuspid Valve Interventions.
Read More →Failure modes in soft-tissue surgical robots: an adjudicated FDA recall cohort, 2005-2026.
Read More →No matching articles.
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