Essentials of European Medical Device Regulatory Affairs

Essentials of European Medical Device Regulatory Affairs
This course will provide an overview of regulatory requirements and considerations for medical devices in a relaxed and interactive environment.

When
:12 June 2024
Time: 9:30-17:00 GMT
Location: TOPRA Office,  6th Floor, 3 Harbour Exchange, London, E14 9GE


Also available as a virtual course, please click here for this registration option.

Course overview 

This course provides an opportunity that on-the-job learning doesn't: network and learn from a variety of experts including your fellow delegates. By attending this course, you will gain a basic understanding of the European medical device regulatory requirements and how to comply with them.


Benefits to delegates

  • Develop a broad understanding of the regulatory affairs profession within the medical devices industry. 
  • Build a network to support the rest of your career
  • Meet and learn from experts in the field   
CPD: This course provides 6 CPD hours upon successful completion. To learn more about why Continuing Professional Development is important, visit our Lifelong Learning page.

Programme

Download a copy of the provisional programme HERE.