The medical device regulation (MDR) has a large impact on the labeling process of many medical organizations worldwide. How technical writers and label designer work together to ensure compliance with the new regulation.
Was der Zuhörer lernt
Insights on the new labeling requirements for medical devices and benefits resulting from the new regulation
Born 1970, degree in Philology Milan (Italy), Ph.D. in Indology Bonn (Germany), since 2001 technical writer, project manager, team lead and associate manager for technical publication at Stryker in Freiburg