Date: 11 July 2024
Time: 16:00 – 16:30 CEST
Language: English
Introduction
The upcoming EU AI Act will have significant implications for medical devices incorporating artificial intelligence. Join our upcoming webinar to explore the key highlights of the new EU AI Act and its impact on the medical device and in vitro diagnostic (IVD) industry. This webinar will delve into the regulatory changes and compliance requirements for manufacturers utilizing artificial intelligence in their products.
The webinar will also include a Q&A. Questions can be sent in advance via the registration form, via marketing@qservegroup.com, or during the webinar.
Who should attend?
This webinar is essential for medical device and IVD manufacturers aiming to enter or continue operating in the European market with AI-driven solutions. It is also highly relevant for healthcare institutions, stakeholders deploying or hosting AI solutions in Europe, and anyone keen to understand the broader implications of the AI Act for the medical sector.
Don't miss this opportunity to stay informed and prepared for the evolving regulatory landscape!
Qserve Host