Company Position Country
Johnson & Johnson Senior Manager, Regulatory Affairs DACH Germany
Session
MDR implementation and suspension: what are the implications?
  • Qualified as a German Lawyer with 20+ years of experience in the regulated health care industry
  • 10 years with Johnson &Johnson Medical, before 10 years with Teleflex Medical
  • Experienced in quality and regulatory affairs in pharmaceutical and mainly medical device industry
  • Expert knowledge of regulatory requirements in the EU and ability to translate regulations into requirements to support CE-marking
  • At J&J involved in the planning and implementation of MDR requirements since 2013
  • Working experience abroad: 1 year in the US (Philadelphia) and 4 years in the UK (London)