- Training
- March 2026
- 1 Day
Global
€774EUR$903USD£649GBP
€893EUR$1,042USD£749GBP
- Directory
- January 2026
Global
- Training
- May 2026
- 2 Days
Middle East, Africa
€1549EUR$1,807USD£1,299GBP
€1788EUR$2,085USD£1,499GBP
- Training
- March 2026
- 2 Days
Asia Pacific
€774EUR$903USD£649GBP
€893EUR$1,042USD£749GBP
- Report
- July 2025
- 120 Pages
Global
From €5280EUR$5,950USD£4,581GBP
- Report
- June 2025
- 150 Pages
Global
From €5280EUR$5,950USD£4,581GBP
- Report
- February 2025
- 133 Pages
Global
From €3549EUR$3,999USD£3,079GBP
- Report
- January 2026
- 183 Pages
Global
From €3495EUR$3,939USD£3,033GBP
- Report
- January 2026
- 185 Pages
Global
From €3495EUR$3,939USD£3,033GBP
- Report
- January 2026
- 188 Pages
Global
From €3495EUR$3,939USD£3,033GBP
- Report
- January 2026
- 185 Pages
Global
From €3495EUR$3,939USD£3,033GBP
- Report
- January 2026
- 193 Pages
Global
From €3495EUR$3,939USD£3,033GBP
- Report
- January 2026
- 191 Pages
Global
From €3495EUR$3,939USD£3,033GBP
- Report
- January 2026
- 193 Pages
Global
From €3495EUR$3,939USD£3,033GBP
- Report
- January 2026
- 188 Pages
Global
From €3495EUR$3,939USD£3,033GBP
- Report
- January 2026
- 183 Pages
Global
From €3495EUR$3,939USD£3,033GBP
- Report
- January 2026
- 199 Pages
Global
From €3495EUR$3,939USD£3,033GBP
- Report
- January 2026
- 183 Pages
Global
From €3495EUR$3,939USD£3,033GBP
- Report
- November 2025
- 180 Pages
Global
From €3495EUR$3,939USD£3,033GBP
- Report
- November 2025
- 199 Pages
Global
From €3495EUR$3,939USD£3,033GBP

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