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Results for tag: "Design History Record"

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3-Hour Virtual Seminar on US FDA and EU Medical Device Directive Requirements for DHF, DMR, DHR and TF/DDS (Recorded) - Product Thumbnail Image

3-Hour Virtual Seminar on US FDA and EU Medical Device Directive Requirements for DHF, DMR, DHR and TF/DDS (Recorded)

  • Training
  • March 2024
  • 3 Hours
  • United States, Europe United States, Europe
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  • 8 Results (Page 1 of 1)
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The Design History Record (DHR) market is a subset of the medical device industry that focuses on the development and maintenance of records related to the design and manufacture of medical devices. DHRs are used to document the design, development, and manufacturing processes of medical devices, and are essential for ensuring the safety and efficacy of these products. DHRs are also used to demonstrate compliance with regulatory requirements, such as those set by the US Food and Drug Administration (FDA). The DHR market is highly competitive, with a range of companies offering products and services related to the design and manufacture of medical devices. These companies provide a variety of services, such as design and development, manufacturing, testing, and regulatory compliance. Some of the major players in the DHR market include Abbott, Becton Dickinson, GE Healthcare, Johnson & Johnson, Medtronic, Philips, Siemens, and Stryker. Show Less Read more