Introduction

The UK has left the EU, and the transition period after Brexit comes to an end this year. From 1 January 2021, all manufacturers placing a medical device on the UK market will first need to register with the Medicines and Healthcare Products Regulatory Agency (MHRA). The new UK regulation and UKCA mark will then apply. In this webinar, we will discuss the new regulations and UKCA. It will still be possible to use CE certificates [MDD/MDR] from European based Notified Bodies until July 2023.

 

Objectives

By the end of the webinar you will understand:

• How to place medical devices on the UK market after 1 January 2021
• How UK medical device manufacturers can continue to supply to the EU market from 1 January 2021
• When to register a medical device with the MHRA
• Understand vigilance, labeling, and role of a UK Responsible Person
• Key dates of changes

 

Agenda

• What are the Medical Devices Regulations and UKCA?
• How it will affect you
• What you need to do and when

 

Target Audience:

• UK medical device manufacturers
• Medical devices manufacturers selling to the UK

 

Cost: No Charge

Language: English UK

 

For further information please contact:  uk.nowisthetime@sgs.com

 

 

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