Adam Sobantka

For the several years, he has been involved in the medical device industry as an auditor, expert, academic lecturer in medical device clinical trials and trainer. He has extensive professional experience. He worked at the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products in the Department of Supervision of Medical Devices, Supervision and Clinical Trials. Between 2011-2016, as an expert of the Ministry of Health and the Registration Authority, he was delegated to work in the European Commission's working groups on MDR and IVDR. In 2014-2016 he was a national expert of the European Commission appointed as a member of the Joint Assessments of European notified bodies in the field of medical devices. From 2016 to 2023, he worked and cooperated with notified bodies in the field of medical devices, as a lead adjudicator, expert and final certification decision maker. He graduated from Jan Długosz Academy in Częstochowa with a degree in Medical Physics and Physics: Computers in Medicine.