Discovering the CE marking process for MDR

The CE marking (MDR) is a legal requirement for companies that intend to place medical devices on the European market. It entails the manufacturer's compliance with the General Safety and Perfomance Requirements (GSPR) outlined in European regulations, ensuring the safety of both devices and patients. During the webinar, the main steps of the CE certification process for MDR will be explained. 

Goal of the webinar

The webinar aims to provide companies with a comprehensive overview of the entire process to achieve CE certification in accordance with the Medical Device Regulation (MDR), from the initial contact until the issue of the certificate, analysing in detail the most critical aspects. Through this session, qualified experts will outline the steps of the certification process, focusing in particular on clinical evaluation and the importance of clinical evidence.

Useful information 

Duration: 11:00 am - 12:00 pm 

Delivery Mode: online 

Course Language: italian