Lecture

Medical Devices Regulation

Description

This lecture covers the European and Swiss regulations on medical devices, including the authorization regime before and after market placement, anti-corruption compliance, and key concepts. It discusses the new legislative framework, the role of the manufacturer, general safety and performance requirements, risk-based controls, post-market surveillance, and the importance of ethical business practices in the industry.

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.