This white paper has been updated to reflect the most recent developments in European Union Medical Device Regulation (MDR) and In Vitro Device Regulation (IVDR) and to bring the current situation into focus.
White paper posts tagged with in vitro device regulation
The European Union Medical Device Regulation (MDR) and In Vitro Device Regulation (IVDR) is a set of standards that governs the production and distribution of medical devices in Europe.
