Zuzanna Kwade is a trainer and consultant to the medical device industry. Zuzanna has over 14 years’ experience of managing pre and post market clinical safety in both devices and pharmaceuticals. In her earlier position, she set up and managed a Clinical Safety Department in a medium-size CRO with focus on medical devices. Currently, Zuzanna is leading clinical evaluation activities for the medical device software products at Agfa Healthcare. She also represents the European Coordination Committee of the Radiological, Electromedical and Healthcare IT Industry (COCIR) in the European Union Task Force on clinical evaluation of software.
Zuzanna holds a PhD in Biochemistry from the university of Antwerp. She is a co-author of several white papers on regulatory aspects of clinical research.