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The MHRA published the response to the consultation on 26th of June 2022

Since the Brexit the UK is building its own regulatory regime to deliver improved patient and public safety, greater transparency, and more proportionate regulation of medical devices. Between September and November 2021, the Medicines and Healthcare products Regulatory Agency (MHRA) consulted on proposed changes to the regulatory framework for medical devices in the United Kingdom (UK). The aim was to seek views on developing future legislation for medical devices.

The MHRA published the response to the consultation on the 26th of June 2022 on the future regulation of medical devices in the United Kingdom. In the document; ‘Government response to consultation on the future regulation of medical devices in the United Kingdom’, published by the MHRA you can read the outcome of the views, what the MHRA has heard, the government’s response to the consultation, and the MHRA’s next steps for the implementation of a transformed regulatory framework for medical devices in the UK.  

Free webinar on the 26th of July
On the 26th of July, Qserve will give you an update to the developments in the free webinar on UK market access; UKCA challenges in uncertain times, hosted by Daniëlle Motta. During this webinar, she will share her experiences as UK Responsible Person and device registrations with the MHRA, address challenges that legal manufacturers are facing with compliance to the UKCA marketing, and more. 

Daniëlle Motta, MSc
Post date: June 25, 2022
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