Martin Grüterich

Martin Grüterich has worked in the medical sector since 2014. Martin began as a Student Research Assistant at the Helmholtz-Institut - RWTH Aachen und Universitätsklinikum Aachen in 2014. In 2016, they completed a Praktikum at Philips. From 2017 to 2021, they worked at ReinVAD GmbH in various roles, including Testengineer, Project Manager RD, and Director QM/RA. Currently, they are the Head of Quality Management and Regulatory Affairs and Senior Quality and Regulatory Affairs Manager at Clinomic.

Martin Grüterich has a Master of Science (M.Sc.) in Elektrotechnik, Informationstechnik und Technische Informatik from RWTH Aachen University, obtained in 2016. Martin also has a Bachelor of Science (B.Sc.) in Elektrotechnik, Informationstechnik und Technische Informatik from RWTH Aachen University, obtained in 2015. In addition, they have obtained several certifications, including IT Security & Datenschutz für Medizinprodukte from Johner Institut GmbH in 2022, Verantwortliche Person PRRC from Johner Institut GmbH in 2022, Risikomanagement und Risikoanalyse für Medizinprodukte nach der ISO 14971:2019 from TÜV SÜD in 2022, Auditor:in der Medizinprodukteindustrie from TÜV Rheinland Group in 2022, DIN EN ISO 27001 - Informationssicherheit für Unternehmen from VIA Consult GmbH & Co. KG in 2022, Fitnesstrainer C-Lizenz from Akademie für Sport und Gesundheit in 2020, and Expert Quality Management Medical Devices International (TÜV) from TÜV Rheinland Group in 2020.