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Quality Management
  • 12.2023 - Training in Technical Documentation according to IVDR at Johner Institut
  • 01.2023 - Training in MDR at Johner Institut
  • 06.2021 - Training in DIN EN ISO 19011:2018 by Tüv Rheinland
  • 02.2020 - Training as PRRC by Johner Institut
  • 03.2018 - Training in Internal Audits for Auditors in the medical device industry in accordance to 13485:2016 and 19011:2011 at TÜV Süd
  • 03.2018 - Training in Quality Management System 13485:2016 at TÜV Rheinland
  • Self trained in EU Medical Device Directive (93/42/EEC)
  • Self trained in US Quality Management System (21 CFR Part 820)