- Conference
- October 2025
- 2 Days
Global
€1600EUR$1,742USD£1,299GBP
€1847EUR$2,011USD£1,499GBP
- Conference
- October 2025
- 1 Day
Global
€800EUR$871USD£649GBP
€923EUR$1,005USD£749GBP
- Conference
- September 2025
- 2 Days
Global
€1600EUR$1,742USD£1,299GBP
€1847EUR$2,011USD£1,499GBP
- Conference
- July 2025
- 2 Days
Global
€1847EUR$2,011USD£1,499GBP
- Conference
- June 2025
- 5 Days
Global
€3325EUR$3,620USD£2,699GBP
€3941EUR$4,291USD£3,199GBP
- Conference
- June 2025
- 2 Days
Global
€1600EUR$1,742USD£1,299GBP
€1847EUR$2,011USD£1,499GBP
- Conference
- June 2025
- 1 Day
Global
€800EUR$871USD£649GBP
€923EUR$1,005USD£749GBP
- Conference
- May 2025
- 2 Days
Global
€1231EUR$1,340USD£999GBP
€1477EUR$1,608USD£1,199GBP
- Report
- January 2025
- 187 Pages
Global
From €3327EUR$3,500USD£2,795GBP
- Report
- February 2025
- 90 Pages
Europe
From €2367EUR$2,490USD£1,989GBP
- Report
- November 2024
- 133 Pages
Europe
From €3803EUR$4,000USD£3,195GBP
- Report
- January 2025
- 133 Pages
Europe
From €3803EUR$4,000USD£3,195GBP
- Report
- October 2024
- 101 Pages
Europe
From €3280EUR$3,450USD£2,755GBP
- Report
- January 2025
- 103 Pages
Europe
From €3280EUR$3,450USD£2,755GBP
- Report
- January 2025
- 103 Pages
Europe
From €3280EUR$3,450USD£2,755GBP
- Report
- September 2024
- 95 Pages
Asia Pacific
From €3280EUR$3,450USD£2,755GBP
- Report
- May 2024
- 102 Pages
Europe
From €3280EUR$3,450USD£2,755GBP
- Report
- November 2023
- 312 Pages
Global
From €4753EUR$5,000USD£3,993GBP
- Directory
- January 2024
- 300 Pages
Global
- Directory
- January 2024
- 200 Pages
Europe

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