UK MHRA Issues More Guidance Ahead Of New Device Regulatory System For 2021
The MHRA has published more guidance on UKRPs and UK product registrations to help medtech companies navigate the new system and continue to reach the market.
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The UK responsible person is the UK equivalent of the Authorized Representative in the EU. MedTech Europe’s Jesús Rueda gives an update on the early experiences of medtech manufacturers seeking to comply with the UK’s new standalone regulations.
Eudamed: Industry Warned That Additional National Actor Registration Requirements Possible While Database Is Voluntary
As manufacturers and other economic operators gets to grips with voluntary registration in the Eudamed database, they need to be prepared for additional registration at national level too.
Three weeks remain for the UK to secure an EU free trade deal, and the transition period will not be extended, the UK government has again underlined.