Further Information
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 join our high level CARAQA
training program, where we will explore the landscape of regulatory
requirements on these and much more topics. Our expert speakers will provide
valuable insights into the regulatory framework for medical devices,
highlighting key considerations for successful market entry and compliance.
On
February 12th, 2024 at
4.30 p.m., 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.