MHRA launches a consultation on indefinite recognition of CE-marked medical devices
MHRA launches a consultation on indefinite recognition of CE-marked medical devices
MHRA launches a consultation on indefinite recognition of CE-marked medical devices
Transitional arrangements and timelines for acceptance of CE marked medical device in Great Britain.
This consultation invites views on proposals for recognising CE marked medical devices in Great Britain.
Reporting, investigating and recalling suspected defective medicinal products to the Defective Medicines Report Centre (DMRC).
Information on the new regulations for the post-market surveillance of medical devices which come into effect on 16 June 2025.