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Results for tag: "Medical Device Reporting"

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Medical Device Complaints, MDR's and Recalls - Product Thumbnail Image

Medical Device Complaints, MDR's and Recalls

  • Training
  • 60 Minutes
  • Global
Be Ready for eMDR Going Live August 14, 2015 - Product Thumbnail Image

Be Ready for eMDR Going Live August 14, 2015

  • Training
  • 110 Minutes
  • Global
UDI Implementation - Product Thumbnail Image

UDI Implementation

  • Training
  • 90 Minutes
  • Global
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Medical Device Reporting (MDR) is a process used by medical device manufacturers to report any adverse events or product problems to the appropriate regulatory authorities. This process is used to ensure the safety and effectiveness of medical devices. It is also used to monitor the performance of medical devices and to identify any potential safety issues. MDR is a critical component of the medical device industry, as it helps to ensure that medical devices are safe and effective for use. Manufacturers must comply with the requirements of the MDR process in order to ensure that their products meet the necessary safety standards. The MDR market is highly competitive, with many companies offering a range of services to help manufacturers comply with the MDR process. These services include consulting, training, and software solutions. Some companies in the MDR market include Medtronic, Johnson & Johnson, Stryker, Becton Dickinson, and Abbott. Show Less Read more