The MHRA is inviting feedback from all stakeholders who may be affected by the proposals, including medical device manufacturers and distributors, trade associations, regulatory experts, approved bodies, healthcare professionals and procurement teams, devolved administrations, and patient representative organisations.
Medical devices regulations: targeted consultation on the indefinite recognition of CE marked devices
The Medicines and Healthcare products Regulatory Agency (MHRA) is inviting feedback on proposals for an approach to indefinitely recognising CE marked medical devices in Great Britain.
This consultation is open until 7th April and members can respond to it here: