The webinar will give information about the MHRA’s intentions for the future medical device regulations, with presentations on:
- updates to the scope of the regulations
- changes to the Classification of General Medical Devices, in vitro Diagnostic Devices and Software as a Medical Device
- changes to Essential Requirements.
This webinar will provide manufacturers, trade associations and healthcare professionals with an opportunity to understand the upcoming updates and to ask questions.
A recording of the webinar will be added to the website post-event for anyone who is unable to attend live.
Should you have any queries concerning the webinar, please email conferences@mhra.gov.uk
You can sign-up here.
