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Anja Friedrich is the head of the Eurofins Medical Device Consulting Team and has more than 25 years of experience in the field of biological safety of medical devices. She herself has set up and performed microbiological studies on medical devices under ISO 17025 and GLP in the laboratory for many years. Specifically, she also supervised validations of reprocessing procedures and has worked on biocompatibility for many years, as well as gaining extensive knowledge of regulatory background and testing strategies through committee work and client projects. Since May 2020, she has been leading the independent Eurofins Consulting company with a team of experts providing advice on the regulatory environment and biosafety of medical devices.