PubMed Literature
Medical device publications from PubMed / NCBI
Biocompatibility assessments for medical devices - evolving regulatory considerations.
Read More →Clinical Evidence Supporting US Food and Drug Administration Premarket Approval of High-Risk Otolaryngologic Devices, 2000-2014.
Read More →Design control considerations for biologic-device combination products.
Read More →Adverse Events Involving Radiation Oncology Medical Devices: Comprehensive Analysis of US Food and Drug Administration Data, 1991 to 2015.
Read More →FDA, CE mark or something else?-Thinking fast and slow.
Read More →Design of Hack-Resistant Diabetes Devices and Disclosure of Their Cyber Safety.
Read More →Spinal devices in the United States-investigational device exemption trials and premarket approval of class III devices.
Read More →The AngelMed Guardian system: Is there a role for implantable devices for early detection of coronary artery occlusion?
Read More →A medical device-grade T1 and ECV phantom for global T1 mapping quality assurance-the T1 Mapping and ECV Standardization in cardiovascular magnetic resonance (T1MES) program.
Read More →Drugs and Devices: Comparison of European and U.S. Approval Processes.
Read More →Clinical trials of lasers for toenail onychomycosis: The implications of new regulatory guidance.
Read More →No matching articles.
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