Explore the latest MedTechLabel research insights on current practices and use scenarios for digital labelling. We will present analysis of real-world digital labelling practices, i) regulatory guidance incl. Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR), ii) initial review of relevant standard on digital device labelling, and iii) survey and desk research findings with digital device labelling perspectives of manufacturers, Notified Bodies and other stakeholders. We will explore updated use scenarios, to illustrate digital device labelling in realistic situations for key medical technology stakeholders. We will discuss storylines and stakeholder-device interactions to make MD/IVD labelling information more palpable.