- Conference
- December 2024
- 5 Days
Global
€2398EUR$2,556USD£1,999GBP
€2998EUR$3,195USD£2,499GBP
- Conference
- June 2024
- 5 Days
Global
€2398EUR$2,556USD£1,999GBP
€2998EUR$3,195USD£2,499GBP
- Report
- February 2022
- 111 Pages
Global
From €5779EUR$5,950USD£4,985GBP
- Report
- April 2024
- 175 Pages
From €4856EUR$5,000USD£4,189GBP
- Webinar
- October 2019
- 120 Minutes
Europe
- Book
- October 2023
- 336 Pages
- Book
- October 2023
- 336 Pages
Medical Device Vigilance is a process of monitoring the safety and performance of medical devices after they have been placed on the market. It involves the collection, analysis, and reporting of adverse events and product problems related to medical devices. This process is essential for ensuring the safety of patients and healthcare professionals.
Medical Device Vigilance is regulated by the European Union and other countries, and is an important part of the medical device industry. Companies must comply with the regulations and report any adverse events or product problems to the relevant authorities. Companies must also keep records of all adverse events and product problems, and take corrective action when necessary.
Some companies in the Medical Device Vigilance market include Abbott, Becton Dickinson, Johnson & Johnson, Medtronic, Philips, Roche, Siemens, and Stryker. Show Less Read more