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Results for tag: "Medical Device Regulation"

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Opportunities in Global Medical Devices & Diagnostics - Product Thumbnail Image

Opportunities in Global Medical Devices & Diagnostics

  • Report
  • October 2019
  • 649 Pages
  • Global
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Introduction to Root Cause Investigation for CAPA - Webinar (Recorded) - Product Thumbnail Image

Introduction to Root Cause Investigation for CAPA - Webinar (Recorded)

  • Webinar
  • February 2019
  • 120 Minutes
  • Global
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The New EU Medical Device Regulation - Webinar (Recorded) - Product Thumbnail Image

The New EU Medical Device Regulation - Webinar (Recorded)

  • Webinar
  • June 2018
  • 60 Minutes
  • Europe
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The Medical Device Regulation market is a sector of the healthcare industry that focuses on the regulation of medical devices. It is responsible for ensuring that medical devices are safe and effective for use in the diagnosis, prevention, and treatment of medical conditions. This includes the development of standards and regulations for the design, manufacture, and distribution of medical devices. The market also includes the monitoring of medical device safety and efficacy, as well as the enforcement of regulations. The Medical Device Regulation market is composed of a variety of stakeholders, including manufacturers, regulatory authorities, healthcare providers, and patients. Manufacturers are responsible for designing, manufacturing, and distributing medical devices, while regulatory authorities are responsible for setting standards and regulations for the industry. Healthcare providers are responsible for using medical devices to diagnose and treat medical conditions, while patients are responsible for using medical devices safely and effectively. Some of the companies in the Medical Device Regulation market include Johnson & Johnson, Medtronic, Abbott Laboratories, Stryker Corporation, and Becton Dickinson. Show Less Read more