Are you interested in the rapidly evolving field of AI-based medical devices? Do you want to stay updated on the latest regulatory challenges and ensure compliance with the U.S. FDA framework? We invite you to attend our exclusive online info event, where we will explore the landscape of regulatory requirements for AI-based medical devices and our expert speakers will provide valuable insights into the U.S. FDA regulatory framework, highlighting key considerations for successful market entry and compliance.
Additionally, we will introduce you to CARAQA – the advanced course about Clinical Affairs, Regulatory Affairs and Quality Assurance. CARAQA is a high-level training program designed to equip professionals with the knowledge and skills needed to navigate the complex regulatory landscape.