PubMed-Literatur
Publikationen zu Medizinprodukten aus PubMed / NCBI
Overview of high-risk medical device recalls in obstetrics and gynecology from 2002 through 2016: implications for device safety.
Mehr lesen →Risk management and regulations for lower limb medical exoskeletons: a review.
Mehr lesen →Stimulating Patient Engagement in Medical Device Development in Kidney Disease: A Report of a Kidney Health Initiative Workshop.
Mehr lesen →Regulation and Device Development: Tips for Optimizing Your Experience With the Food and Drug Administration.
Mehr lesen →Ford and Edison in a modern regulatory environment: the first-in-human trial of night-work and artificial light.
Mehr lesen →Orthopaedic Device Approval Through the Premarket Approval Process: A Financial Feasibility Analysis for a Single Center.
Mehr lesen →Innovative postmarket device evaluation using a quality registry to monitor thoracic endovascular aortic repair in the treatment of aortic dissection.
Mehr lesen →Medical Device Recalls in Radiation Oncology: Analysis of US Food and Drug Administration Data, 2002-2015.
Mehr lesen →Print Me an Organ? Ethical and Regulatory Issues Emerging from 3D Bioprinting in Medicine.
Mehr lesen →Mechanical performance of cervical intervertebral body fusion devices: A systematic analysis of data submitted to the Food and Drug Administration.
Mehr lesen →Biocompatibility assessments for medical devices - evolving regulatory considerations.
Mehr lesen →Keine passenden Artikel.
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