white paper & case studies

White paper posts tagged with in vitro device regulation

UPDATE to The Clock Is Ticking: Will Notified Body Capacity for the EU MDR Affect You?
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.
The Clock Is Ticking: Will Notified Body Capacity for the EU MDR Affect You?
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.