Are you an innovative sSME in the regulatory affairs, medical devices and/or quality management system fields? We have a challenge for you!
MDR-prep, an innovative electronical QMS-tool for compliance to the Medical Device Regulation (MDR) of early-stage medical device development, providing of intuitive templates and guidance through Standard Operating Procedures (SOP). This guarantees MDR compliance of investigational medical device research and prevents incomplete dossiers and re-doing critical tests at a later stage saving time and assure proper use of funding.
Watch the recording of the MDR-prep Open Market Consultation event to learn how to pilot a solution with Delft University of Technology: