Section 1
Further Information
With a 360-degree learning experience, CARAQA (Clinical Affairs, Regulatory Affairs and Quality Assurance) strikes a balance between theoretical aspects and hands-on practice. You will gain advanced knowledge from university experts, medtech professionals and industry representatives, empowering you to take on the role of a person responsible for regulatory compliance (PRRC) within your company.
Developed in collaboration with Lübeck University of Applied Sciences and Medidee SA, this training program offers a unique opportunity designed to ensure a smooth transition to the requirements under MDR/IVDR.
During the online info event, our experts, Prof. Spitzenberger of TH Lübeck and Dr. Elena Lucano of Medidee Services SA, will provide valuable insights into the course content. They will also discuss organizational topics, such as discount opportunities, as well as the structure of the course, which combines online and onsite training.
