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)