| answer text |
<p>The Medicines and Healthcare products Regulatory Agency (MHRA) is will conduct
a public consultation this summer on the future medical device regulatory regime.
This consultation will inform future amendments made to the United Kingdom Medical
Device Regulations 2002 as required under the Medicines and Medical Devices Act 2021.
The public consultation will cover various aspects of the medical device regulations,
including requirements relating to clinical investigations and evidence. The MHRA
is committed to ensuring that both pre- and post-market standards are enhanced to
protect UK patients whilst supporting innovation with greater alignment with international
standards for pre-market clinical data. This will ensure that the domestic medical
devices regime remains fit for purpose in an evolving public health environment and
facilitates a sector that embraces innovation.</p>
|
 |
