Lecture
Medical Device Development and Regulation in Europe and US
Description
This lecture covers the development and regulation of medical devices in Europe and the US, focusing on the transition from old directives to new regulations, compliance requirements, the role of Notified Bodies, and the impact of Brexit and other geopolitical events. It also discusses the use of international standards for compliance, the three pillars of compliance based on technical, biological, and clinical aspects, and the career opportunities in the medical device industry.
Official source
About this result
This page is automatically generated and may contain information that is not correct, complete, up-to-date, or relevant to your search query. The same applies to every other page on this website. Please make sure to verify the information with EPFL's official sources.