David Sooprayen

David Sooprayen possesses extensive experience in regulatory affairs and clinical evaluation within the medical devices sector. Currently serving as the Head of Regulatory Affairs at Sonova Gruppe since February 2013, David has held multiple key positions, including Senior Manager and Regulatory Affairs Manager, where responsibilities encompassed EU certification, MDSAP, and compliance with the Medical Device Regulation (MDR). Previous roles include Regulatory Clinical Affairs Manager, focusing on clinical evaluation and study design, as well as Validation Project Manager. David's career in audiology began with positions as a Certified Hearing Aid Specialist at Mahlke Hörakustik and Fischer Optik-Akustik GmbH. Academically, David holds a Master of Science in Clinical Research from the Universität für Weiterbildung Krems, and a Bachelor of Science in Audiology & Hearing Technology from Technische Hochschule Lübeck, supplemented by comprehensive vocational training in audiology and hearing acoustics.