PubMed Literature
Medical device publications from PubMed / NCBI
The Essential Role of Medical Monitors in Clinical Trials.
Read More →Global trends in post-market surveillance of high-risk medical devices: An empirical analysis based on regulatory data.
Read More →Regulatory and Legal Considerations with Artificial Intelligence in Dermatology.
Read More →Regulatory Fragmentation in Europe and Its Risks for Patient Access and Safety: Subcontracting Work Flow Steps of In-House Diagnostic Procedures.
Read More →Confirmatory evidence supporting single pivotal trial new drug approvals by the Food and Drug Administration, 2015 through 2023.
Read More →Evaluation of nickel release from Ni-Ti stents in various media for safety assessment purposes.
Read More →Use of Bayesian decision analysis in the design of patient-centered clinical trials for kidney failure devices.
Read More →Clinical characteristics and prognostic factors analysis in patients with post-neurosurgical intracranial infection caused by Acinetobacter baumannii.
Read More →Navigating through regulatory frameworks for digital therapeutics and biomarkers.
Read More →Regulatory Adoption of AI, ML, Computational Modeling & Simulation in In-Silico Clinical Trials for Medical Devices: A Systematic Review.
Read More →Relevant domains for health technology assessment of medical device reimbursement in Brazil's unified health system: a survey and Delphi panel study on stakeholder preferences.
Read More →No matching articles.
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