New Medtech EU MDR/IVDR regulations
Type of event: Offline event
The event highlights the new EU regulations for medical devices (MDR) and in vitro diagnostics (IVDR) in their entire scope and shows possible solutions - especially for SMEs.
The new EU regulations for medical devices (MDR) and in vitro diagnostics (IVDR) published at the end of May pose major operational and strategic challenges for the entire industry. This event, which is jointly organised by HTCS and BaselArea.swiss, will explore the current situation and bring together leading experts from industry and the service sector.
All content loaded