의료기기 이야기

As previously reported, during a public consultation launched in November 2024, the UK medical device regulator, the Medicines and Healthcare products Regulatory Agency (MHRA), proposed removing the revocation dates of four pieces of assimilated EU law so that they remain part of the statutory framework for medical devices in Great Britain (GB) until they are replaced with the updated UK law. U..

On September 18, Robert Reid, Ph.D. Deputy Director, Innovative Devices at the Medicines and Healthcare products Regulatory Agency (MHRA), updated the RAPS audience on the current status of the UK legislation. To our knowledge, this is one of the most recent updates from the MHRA. The first half of 2024In January 2024, the MHRA shared a roadmap for 2024-2025. The roadmap proposed regulatory refo..