News / Blogs
MHRA grants 1 year extension for UKCA Compliance
Understanding UKCA marking and labelling requirements in Northern Ireland
Understanding UKCA marking and labelling requirements for Great Britain
Deadline to appoint a CH-REP for Class 1 & System/Procedure packs is approaching
The deadline for appointing a Swiss Authorised Representative (CH-REP) for Class 1 Devices, and System/Procedure Packs is fast approaching.
Medical Device Regulations in the UK: An Overview
The Medicines & Healthcare products Regulatory Agency (MHRA) has been responsible for medical device and pharmaceutical regulations in the United Kingdom since 2003
What is the UK Conformity Assessed Mark (UKCA)?
The United Kingdom Conformity Assessed (UKCA) mark is replacing the CE mark in Great Britain, as the United Kingdom left the EU single market on 31 December 2020.
