Global Medical Devices and In-Vitro Diagnostic companies are all gearing up for the new EU MDR/IVDR regime. Only a top few medical devices companies have managed to win the race while others are struggling to meet the new regulatory requirements. As the industry is moving closer to final application deadline, there are new challenges related to maintaining and sustaining regulatory compliance. Learn how Atos has helped large organizations meet these new regulatory requirements as part of EU MDR/ IVDR compliance programs.