This webinar will focus on the process involved with the release of new medical devices.
In this second of the webinar of the series, From research and innovation to development: how to plan and execute translational projects in life sciences, the BioMedical SIG invites you to discuss the development of medical devices.
Mattia Ronchetti, Senior Director Global Clinical and Regulatory Affairs from BVI Medical, will explain the regulatory path for medical devices approval.
The webinar will introduce the basic concepts of the current European medical device regulatory framework according to Regulation EU 2017/745 (MDR), and its main similarities and differences with the US regulatory environment. The importance and value creation of developing a regulatory and clinical strategy in early stage projects will be addressed.
This webinar is organised by the BioMedical SIG. Join the BioMedical SIG to stay informed.
