In our upcoming stakeholder webinar, we will introduce our work  – and hear from stakeholders about their challenges and wishes.

Participants will learn more about MedTechLabel’s aim to create a unified labelling specification for all categories and classes of medical devices and in vitro diagnostics. The session will explore concrete use scenarios that could benefit from digital labelling and provide an opportunity for stakeholders to share their perspectives, needs, and expectations regarding digital medical labelling.

We extend the invitation to stakeholders from across the medical devices and in vitro diagnostics ecosystem, including manufacturers, Notified Bodies, regulators, policy makers, healthcare providers, healthcare professionals, and patients. Participants will also be invited to engage with the project and contribute to the ongoing dialogue on how digital labelling can support safer, more accessible, and more effective use of medical devices and in vitro diagnostics.