- Report
- August 2021
- 111 Pages
Middle East, Africa
From €3098EUR$3,450USD£2,638GBP
- Report
- December 2023
- 114 Pages
Global
From €3995EUR$4,450USD£3,402GBP
- Report
- December 2023
- 79 Pages
Europe
From €3367EUR$3,750USD£2,867GBP
- Report
- April 2024
- 140 Pages
Global
From €4443EUR$4,949USD£3,784GBP
- Report
- June 2023
- 111 Pages
Global
From €4040EUR$4,500USD£3,441GBP
- Report
- November 2022
- 29 Pages
Global
From €1751EUR$1,950USD£1,491GBP
- Report
- January 2022
- 24 Pages
Global
From €1751EUR$1,950USD£1,491GBP
- Training
- November 2025
- 1 Day
Global
€425EUR$490USD£350GBP
€486EUR$560USD£400GBP
- Report
- April 2025
- 22 Pages
Global
From €265EUR$295USD£226GBP
From €893EUR$995USD£761GBP
- Training
- December 2025
- 2 Days
Russia
€1579EUR$1,820USD£1,299GBP
€1822EUR$2,100USD£1,499GBP
- Training
- July 2025
- 2 Days
Russia
€1579EUR$1,820USD£1,299GBP
€1822EUR$2,100USD£1,499GBP
- Report
- May 2024
- 102 Pages
Europe
From €3098EUR$3,450USD£2,638GBP
- Report
- November 2023
- 94 Pages
Europe
From €3098EUR$3,450USD£2,638GBP
- Report
- November 2023
- 122 Pages
Europe
From €3098EUR$3,450USD£2,638GBP
- Report
- January 2023
- 169 Pages
Global
From €2245EUR$2,500USD£1,912GBP
- Webinar
- February 2022
- 6 Hours
Europe
From €534EUR$595USD£455GBP
- Training
- 60 Minutes
Europe
- Training
- 90 Minutes
Europe
From €494EUR$550USD£421GBP

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