The European In-Vitro Diagnostics Regulation

With the IVDR coming into force, manufacturers and developers of in vitro diagnostics and biomarkers must comply with the new regulatory requirements. Many companies, especially small and medium-sized enterprises, face major hurdles in this transition. With this condensed introduction to the IVDR, the two networks the Interreg North-West Europe Codex4SMEs and Interreg Baltic Sea BiC want to offer SMEs some guidance on how to get started. Attendees will receive an exclusive tutorial for the Biomarker Commercialization Guide and the IVDR Guide of the BIC project. To make new contacts, the event offers all participants the opportunity for one-to-one meetings during the networking session.