The rules changed since the implementation of Medical Device Regulation (MDR) 2017/745, and it is time to talk about what really happens when you’re monitoring medical devices’ vigilance after they hit the market. Our webinar, “From Theory to Reality,” gives an analysis of our experience and a review of the actual ups and downs of setting up a Post-Marketing Surveillance (PMS) system.
Watch Asphalion expert Laura Eder diving into the opportunities that will bring you building up your Post-Marketing Surveillance System.
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As a company committed to sustainability, we follow the UN’s 2030 Agenda and its Sustainable Development Goals.
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