Questions and Answers on vigilance terms and concepts as outlined in the Regulation (EU) 2017/745 on medical devices

Information

Type

Guidance

Regulated products

Medical Devices

Topics

Post-Market Surveillance And Vigilance (PMSV)

Published

February 1, 2023

Last updated

February 1, 2023

Description

This document provides an overview of vigilance terms and concepts in the EU regulation on medical devices, focusing on post-market surveillance.

Organization

Country / Region

European Union

License

Creative Commons Attribution 4.0

Feedback

Suggest an improvement to this page

Actions

Social networks

Embed