Great Britain
The new article provides additional clarifications regarding the upcoming changes to the UK regulatory framework.
European Commission
The new article provides additional clarifications regarding the specific scope of information-related obligations medical device manufacturers should comply with.
European Commission
The article highlights the key points related to the manufacturers’ obligations in case of product supply being interrupted or discontinued.
Saudi Arabia
The article outlines the basics of the regulatory framework for innovative medical devices.
Australia
The article highlights the key points associated with notifications for certain types of medical devices in the context of their specific regulatory nature.
FDA
The new article explains the approach to be followed in the context of retention and management of electronic records.
