PubMed Literature
Medical device publications from PubMed / NCBI
Impact1: Supporting Innovation in Pediatric and Maternal Health-5 Years of Outcomes.
Read More →Global pharmacovigilance reporting: comparative analysis of adverse event obligations across five major regulatory authorities.
Read More →A Perspective for Integrating Real-World Evidence Into the Investigational Device Exemption Study Design for Lumbar Total Joint Replacement.
Read More →Analysis of Trends in FDA-Recalled Hip Arthroplasty Devices: A Retrospective Review.
Read More →Cybersecurity breaches in medical devices: analyzing FDA safety communications in response to patient security concerns.
Read More →A Multidimensional Index Framework for Evaluating the Regulatory Applicability of ISO 10328 Using a Prosthetic Knee Case Study.
Read More →Urologic Device Innovation and Trends: An Analysis of Food and Drug Administration Approvals From 1990 to 2023.
Read More →Medical Device Regulation - Who Does the FDA Serve?
Read More →Device failures and patient adverse events from EUS: 26-year FDA MAUDE analysis (2000-2025).
Read More →Artificial intelligence as medical device in radiology in 2025: the regulatory scenario in the EU, USA, and China.
Read More →Clinical Trial Design and Regulatory Requirements for Artificial Intelligence as a Medical Device: A PRISMA-ScR-Guided Scoping Review of Global Guidance and Evidence (2017-2025).
Read More →No matching articles.
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