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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
:11 June 2025
Time:
9:30-17:00
GMT
Location
: TOPRA Office, London
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
.