PubMed-Literatur
Publikationen zu Medizinprodukten aus PubMed / NCBI
Pediatric Medical Device Development and Regulation: Current State, Barriers, and Opportunities.
Mehr lesen →Regulatory strategies for early device development and approval.
Mehr lesen →Summary of the FDA virtual public workshop on spinal device clinical review held on September 17, 2021.
Mehr lesen →Prospective Pilot Study of Robotic-Assisted Harvest of the Latissimus Dorsi Muscle: A 510(k) Approval Study with U.S. Food and Drug Administration Investigational Device Exemption.
Mehr lesen →The current status of breakthrough devices designation in the United States and innovative medical devices designation in Korea for digital health software.
Mehr lesen →Eine vergleichende Studie über regulatorische Perspektiven auf innovative medizinische Geräte in Korea und den Vereinigten Staaten.
Mehr lesen →Recalls of Moderate- and High-Risk Otolaryngologic Devices Approved by the US Food and Drug Administration, 2003-2019.
Mehr lesen →Navigating the Regulatory Pathway for Medical Devices-a Conversation with the FDA, Clinicians, Researchers, and Industry Experts.
Mehr lesen →The power of public-private partnership in medical technology innovation: Lessons from the development of FDA-cleared medical devices for assessment of concussion.
Mehr lesen →New Insights into MR Safety for Implantable Medical Devices.
Mehr lesen →Interpretation of regulatory factors for 3D printing at hospitals and medical centers, or at the point of care.
Mehr lesen →Keine passenden Artikel.
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