Description: The UK medical devices regulatory landscape is changing at a rapid rate, with an increasingly more complex environment than ever before.
This panel will share insights on known and anticipated UK regulatory requirements while the future UK Medical Devices Regulation (UK MDR) is in development.
The attendees will gain an understanding of the Approved Body perspective of current UK regulatory requirements for medical devices and IVDs which will aid them to navigate their path to compliance.
In addition, this session will provide discussion of recent developments relating to the future UK MDR enabling the attendee to interpret these requirements for their organisation and products.
Learning Objectives:
Understand the regulatory structure in the UK for medical devices
Have awareness of anticipated changes to the UK Medical Devices Regulations
Understand the UK Approved Body perspective of compliance with UK regulations
