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New MHRA device registration guidance & updated BDIA FAQ document

08 December 2020

The MHRA has published new guidance on how to register as a manufacturer to sell medical devices on the Great Britain and Northern Ireland markets from 1 January 2021. 

The guidance contains information on what devices will need to be registered, how the registration process will work and how these requirements differ between Great Britain and Northern Ireland. 

Included is a collection of detailed reference documents and video tutorials designed to guide companies through the registration process.

We have also updated our Frequently Asked Questions document to take the new guidance into account, and this is available below. 

Read the MHRA Guidance

Download the FAQ

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