Webinar: UK MHRA Medical Devices & IVDs registration process

As of 1 January 2021, all non-UK based manufacturers are required to nominate a UK Responsible Person to place their Medical Devices & In-Vitro Diagnostics Devices on the UK market.

In this webinar, we will be providing you with information about the MHRA registration in relation to:​

• How to register your devices to the portal
• The Authorities’ specific requirements
• Timeline
• Expenses