PubMed Literature
Medical device publications from PubMed / NCBI
A NEW HEALTH TECHNOLOGY ASSESSMENT SYSTEM FOR DEVICES: THE FIRST FIVE YEARS.
Read More →Incremental Revisions across the Life Span of Ophthalmic Devices after Initial Food and Drug Administration Premarket Approval, 1979-2015.
Read More →Overview of high-risk medical device recalls in obstetrics and gynecology from 2002 through 2016: implications for device safety.
Read More →Risk management and regulations for lower limb medical exoskeletons: a review.
Read More →Stimulating Patient Engagement in Medical Device Development in Kidney Disease: A Report of a Kidney Health Initiative Workshop.
Read More →Regulation and Device Development: Tips for Optimizing Your Experience With the Food and Drug Administration.
Read More →Ford and Edison in a modern regulatory environment: the first-in-human trial of night-work and artificial light.
Read More →Orthopaedic Device Approval Through the Premarket Approval Process: A Financial Feasibility Analysis for a Single Center.
Read More →Innovative postmarket device evaluation using a quality registry to monitor thoracic endovascular aortic repair in the treatment of aortic dissection.
Read More →Medical Device Recalls in Radiation Oncology: Analysis of US Food and Drug Administration Data, 2002-2015.
Read More →Print Me an Organ? Ethical and Regulatory Issues Emerging from 3D Bioprinting in Medicine.
Read More →No matching articles.
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