Regulation (EU) 2017/745: what changes for medical device traceability?

Loss of traceability of DMs poses a serious health risk to patients and users. The new European Parliament Regulation provided a common strategy, based on internationally recognized principles, through the establishment of a unique device identification system (UDI system). Read the full article…

Date: 06.2020   Source:

Leave a Comment

Your email address will not be published. Required fields are marked *

This site uses Akismet to reduce spam. Learn how your comment data is processed.