Hasmik Kirakosyan is a regulatory affairs professional specializing in European medical device regulations, market access, and Authorized Representative activities. As a Regulatory Affairs Specialist at Masimo in Switzerland and PRRC for its Swiss Authorized Representative, she leads European market entry initiatives and provides training on EU MDR economic operator requirements. Prior to joining Masimo, she spent five years at MDSS GmbH in Germany, where she established and led the Swiss Authorized Representative service. Hasmik is a recurring speaker at industry conferences, including Swiss Medtech and this conference, where she returns following her presentation in 2025 to share practical insights on the implementation of the EU M