Fortbildungen/Zertifikate:
- MDR/IVDR Expert (en.co.tec)
- PRRC (Person Responsible for Regulatory Compliance, en.co.tec)
- Sufficient Clinical Evidence under MDR (EU) 2017/745 (Qunique GmbH)
- 13. medical device forum (TÜV SÜD Akademie)
- ISO 13485:2016 ? Quality Management System Medical Devices (BSI Training Academy)
- EU-Verordnung 2017/745 für Medizinprodukte (MDR) (BSI-en.co.tec)
- FDA 510(k) Workshop in Amsterdam (Medical Device Academy, Inc.)
- Validation of Sterile Medical Devices Seminar (Nelson Labs)
- 2nd Annual Drug/Device Combination Products Summit (Qepler S.R.O.)
- Medical Device Regulation 2017/745 (MDR) im Detail (TÜV SÜD Akademie)