Implementation of medical devices future regime
Page summary:
A roadmap outlining the intended timelines for delivering a future regulatory framework for medical devices and an intended policy on international recognition.
Change made:
Updated to include a link to the MHRA’s Consultation on Medical Devices Regulations: Routes to market and in vitro diagnostic devices, and to update the list of topics to be included in the ‘pre-market’ regulations.
Time updated:
12:01am, 14 November 2024
Consultation on Medical Devices Regulations: Routes to market and in vitro diagnostic devices
Page summary:
The MHRA is inviting members of the public to provide their views on proposed changes to the regulatory framework for medical devices.
Change made:
First published.
Time updated:
12:01am, 14 November 2024
The MHRA seeks views on pre-market regulations for medical devices to improve patient access and strengthen patient safety
Page summary:
Responses will help shape reforms that will boost UK patients’ access to safe and innovative medical products
Change made:
First published.
Time updated:
9:14am, 14 November 2024
Clinical Trials Regulations webinar recordings
Page summary:
Webinar recordings providing information about plans for implementing the new Clinical Trial Regulations.
Change made:
First published.
Time updated:
2:17pm, 13 November 2024
