PubMed Literature
Medical device publications from PubMed / NCBI
Comparative analysis of medical device adverse event reporting forms for patients and industries across various countries, and the introduction of a unified generic form for harmonization.
Read More →Could one strategy fit all? A comparison of regulatory guidance from China, Europe, and the USA on medical device clinical evaluation throughout the total product lifecycle.
Read More →Regulatory gaps in India's medical device framework: The case of Johnson and Johnson's faulty hip implants.
Read More →From Registry to Reality: Opportunities to Enhance Post-market Surveillance of High-Risk Medical Devices Comment on "Quality and Utility of European Cardiovascular and Orthopaedic Registries for the Regulatory Evaluation of Medical Device Safety and Performance Across the Implant Lifecycle: A Systematic Review".
Read More →US regulatory compliance for medical combination products: an overview.
Read More →How to improve the mechanical safety of a novel spinal implant while saving costs and time.
Read More →No matching articles.
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