Seminar: Placing Medical Devices and IVDs on the Union Market


    • EU MDR/IVDR Status Update – Where do we stand 1 year after the date of application? 
    • Lessons learned with the implementation of economic operators’ requirements & Technical Documentation expectations
    • Lessons learned with EU MDR/IVDR Initial Audit Process 
    • Clinical/Performance Evaluation and PMCF/PMPF expectations of notified bodies 
    • Q&A Session (Panel Discussion)
24-hour access - 20€
48-hour access - 45€
Unlimited access - 100€