Oleg Repp is an expert in clinical evaluation of medical devices in accordance with the MDR, MDCG guidance documents and MEDDEV 2.7/1 Rev. 4. He plans and conducts scientific literature searches, evaluates PMS and PMCF data, and supports the regulatory classification of medical device software. Prior to joining Metecon, he was responsible for post-market surveillance and clinical study coordination in the field of orthopaedics.
