PubMed Literature
Medical device publications from PubMed / NCBI
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 →Regulatory landscape of accelerated approval pathways for medical devices in the United States and the European Union.
Read More →The FDA's Pivotal Role in Global Therapeutic Product Availability.
Read More →Multipurpose prevention technologies for the prevention of unintended pregnancy, HIV, and other sexually transmitted infections: regulatory pathways and challenges.
Read More →Generative AI's healthcare professional role creep: a cross-sectional evaluation of publicly accessible, customised health-related GPTs.
Read More →A deployment safety case for AI-assisted prostate cancer diagnosis.
Read More →No matching articles.
Page 11 of 43