In this webinar, our managing director Patrick Pfau was talking about how medical device manufacturers can deal with the increasing number of regulatory authorities worldwide and how they can setup a global and company-wide strategy for UDI.
The webinar started with an overview on the status-quo of UDI worldwide and future requirements. In addition, Patrick Pfau talked about what it takes to prepare globally for UDI and he also gave insights into an approach to achieve and maintain global UDI compliance for UDI. Using the UDI Platform as an example, he finally showed how data for different authorities can be managed in one system.
Request webinar recording and presentation here.