Lecture

Medical Devices Regulation

In course

Amet commodo quis et exercitation dolor nisi dolor dolor eiusmod non in nostrud. Excepteur ea in sint nostrud Lorem ex aute occaecat cupidatat cupidatat ea Lorem ipsum. Dolore magna cillum reprehenderit pariatur duis et et. Aute et aliqua elit eu enim eu tempor do ipsum in commodo. Ipsum elit sit eiusmod deserunt laboris id in nulla sint qui nulla excepteur est proident.

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.

Official source

https://mediaspace.epfl.ch/media/0_4ojbnu5y

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.

Ontological neighbourhood

Related lectures (34)

Graph Chatbot

Chat with Graph Search

Ask any question about EPFL courses, lectures, exercises, research, news, etc. or try the example questions below.

DISCLAIMER: The Graph Chatbot is not programmed to provide explicit or categorical answers to your questions. Rather, it transforms your questions into API requests that are distributed across the various IT services officially administered by EPFL. Its purpose is solely to collect and recommend relevant references to content that you can explore to help you answer your questions.