No. ICS only functions as a Contract Research Organization (CRO) for the planning, conduct, and evaluation of the clinical performance study. CE-certification can only be carried out by accredited notified bodies. Currently (September 2023), there are twelve notified bodies designated under IVDR 2017/746: DEKRA Certification GmbH (Germany), DEKRA Certification B.V. (Netherlands), TÜV SÜD Product Service GmbH (Germany), TÜV Rheinland LGA Products GmbH (Germany), BSI Group The Netherlands B.V. (Netherlands), GMED SAS (France), National Standards Authority of Ireland (Ireland), MDC Medical Device Certification GmbH (Germany), 3EC International a.s. (Slovakia), QMD Services GmbH (Austria), Eurofins Electric & Electronics Finland Oy (Finland), and Sertio Oy (Finland). Please consider the individual scope of IVD-products that the individual notified bodies are accredited for.