CEO, Pure Clinical
For 12 years associated with the medical devices industry/sector/market as an auditor, expert, university lecturer in the field of clinical trials of medical devices and a trainer. July 2021 to February 2022 employed at TÜV Nord Polska as a Business Development Manager responsible for the development of medical device certification service. In the years 2016- 2021, the Director of the Department for the Certification of Medical Devices at the Polish Center for Testing and Certification S.A. Co-author of the book Clinical Research in Poland.
A graduate of Jan Długosz University in Częstochowa in the fields of Medical Physics and Physics: Computers in Medicine. Former employee of the Ministry of Health in the Department of Drug Policy and Pharmacy and the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products in the Department of Medical Devices Surveillance, Vigilance and Clinical Trials . In 2011-2016, an expert of the Ministry of Health and the Registration Office delegated to work in the European Commission working groups for MDR and IVDR. In 2014-2016, a national expert of the European Commission appointed as a Joint Assessments of European notified bodies in the field of medical devices, members.