DRSConsult Dr. Thomas Schlieper

The core activity of DRS Consult is to advise and support companies in the field of medical devices, particularly in complying with regulatory requirements such as the MDR (Medical Device Regulation) and the IVDR (In Vitro Diagnostic Regulation). This also includes audits, supporting the implementation of quality management systems (ISO 13485) and risk management (ISO 14971), as well as representing companies as importers or representatives in Switzerland and the United Kingdom.