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mhra 1 year extension ukca compliance

MHRA grants 1 year extension for UKCA Compliance

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Understanding UKCA marking and labelling requirements in Northern Ireland

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understanding ukca marking and labelling for northern ireland
Understanding UKCA marking and labelling requirements for Great Britain

Understanding UKCA marking and labelling requirements for Great Britain

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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.
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Swiss flag on a flagpole with mountains behind and a blue sky, to represent CH-REP deadline
two doctors in scrubs, masks and glasses in an operating theatre to represent the use of medical devices

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
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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.
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UKCa logo - what is the ukca conformity mark

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