As of May 2020, confinis ag- senior adivsorduring my Swiss Medtech time- 2017 regulatory expert and lead coordinator of the SIT (the MDR/IVDR Swiss implementation task force) - 2017-2020 Head of Regulatory Affairs During my Swissmedic time member/participant- European Notified Bodies Operation Group (NBOG)- European Competent Authority for Medical Devices (CAMD)- Coordination Group (CG), a NBOG subgroup mainly coordinating the NB joint assessments- (MDR/IVDR) Implementation task force degree in mechanical engineering - industrial experience with medical devices goes back to 1992 (core activities: hip implants)- 2008-2012 Head of Market Surveillance Medical Devices, Swissmedic- 2012-2017 Senior Expert Regulation and Compliance Medical Devices, Swissmedic- since May 2017 Senior Expert Regulation, Swiss Medtech (Swiss trade association representing medical technology industries)