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

Register and get the recording!

Sign Up!

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