The European MDR has replaced MDD and lead to many changes in the industry including changes in the labelling, IFU & UDI rules. TT Group worldwide helps you gain knowledge about these changes and their implementation. Through the most experienced speakers, industry executives will gain insights on device safety and clinical effectiveness, and the effective measures to comply with data transparency to be shared via EUDAMED & Instructions for use (IFUs).
This two-day conference will provide the participants within depth learning/knowledge on the label content changes, IFU changes and the other key highlights of the implication of MDR transition. Through presentations, interactive group discussions and panel discussions this meeting aims at addressing the concerns about the changes occurred in each area of European Medical Device Labelling, IFU, UDI.