Reporter’s occupation and source of adverse device event reports contained in the FDA’s MAUDE database

Eitemau Tebyg

• The Dangers of Dental Devices as reported in the FDA MAUDE Database
  gan: Hebballi, Nutan B, et al.
  Cyhoeddwyd: (2015)
• A Primer to the Structure, Content and Linkage of the FDA’s Manufacturer and User Facility Device Experience (MAUDE) Files
  gan: Ensign, Lisa Garnsey, et al.
  Cyhoeddwyd: (2017)
• Biclustering of Adverse Drug Events in FDA’s Spontaneous Reporting System
  gan: Harpaz, Rave, et al.
  Cyhoeddwyd: (2010)
• Reducing Glucose Meter Adverse Events by Using Reliability Growth With the FDA MAUDE Database
  gan: Krouwer, Jan S.
  Cyhoeddwyd: (2018)
• Large Eddy Simulation of FDA’s Idealized Medical Device
  gan: Delorme, Yann T., et al.
  Cyhoeddwyd: (2013)