Director Europe, Quality Systems & Regulatory Affairs - Johnson & Johnson
Global Impact of EU MDR/IVDR
Wednesday 31 May 16:20 - 17:10
Prior to joining Johnson & Johnson, Peter began his career in the chemical industry. In the Medical Devices industry, he set up manufacturing and servicing structures for active and passive medical devices, lead Quality System and Product certification programs according to international standards, national and EU Medical Device regulations.
He is the Vice Chair of the MedTech Europe Regulatory Affairs Council, member of the R&I Committee and an active member of several working groups.