Our focus: MDR consulting and services for medical devices such as quality management, risk management, clinical data and studies or clinical evaluation. Project overview: 45+ medical device projects (from idea to product) 120+ dossiers 20+ patents Competence status Certified according to DIN EN ISO 13485:2016, Medical Device Regulation (MDR), Medical Device Law Implementation Act (MPDG), expert knowledge in GCP and GMP as well as ISO 14155 and always up-to-date specialist knowledge. About the company: Founded in 2003 10+ in-house specialists a large number of satisfied customers Project partners: Mediconomics GmbH (Europe/USA/Canada) DNV MedCert GmbH (Germany)